ID22905A - Pembuatan n-butiraldehida dan/atau n-butanol - Google Patents

Pembuatan n-butiraldehida dan/atau n-butanol

Info

Publication number
ID22905A
ID22905A IDW990822A ID990822A ID22905A ID 22905 A ID22905 A ID 22905A ID W990822 A IDW990822 A ID W990822A ID 990822 A ID990822 A ID 990822A ID 22905 A ID22905 A ID 22905A
Authority
ID
Indonesia
Prior art keywords
pct
adduct
butanol
date sep
butyraldehyde
Prior art date
Application number
IDW990822A
Other languages
English (en)
Inventor
Kanand Jurgen
Roper Michael
Paciello Rocco
Original Assignee
Basf Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Basf Ag filed Critical Basf Ag
Publication of ID22905A publication Critical patent/ID22905A/id

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00—Compounds having —CHO groups
    • C07C47/02—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C07C41/05—Preparation of ethers by addition of compounds to unsaturated compounds
    • C07C41/06—Preparation of ethers by addition of compounds to unsaturated compounds by addition of organic compounds only
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C07C41/32—Preparation of ethers by isomerisation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/48—Preparation of compounds having groups
    • C07C41/50—Preparation of compounds having groups by reactions producing groups
    • C07C41/54—Preparation of compounds having groups by reactions producing groups by addition of compounds to unsaturated carbon-to-carbon bonds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C07C45/511—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
    • C07C45/515—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being an acetalised, ketalised hemi-acetalised, or hemi-ketalised hydroxyl group

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
IDW990822A 1997-03-17 1998-03-06 Pembuatan n-butiraldehida dan/atau n-butanol ID22905A (id)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19710994A DE19710994A1 (de) 1997-03-17 1997-03-17 Verfahren zur Herstellung von n-Butyraldehyd und/oder n-Butanol

Publications (1)

Publication Number Publication Date
ID22905A true ID22905A (id) 1999-12-16

Family

ID=7823624

Family Applications (1)

Application Number Title Priority Date Filing Date
IDW990822A ID22905A (id) 1997-03-17 1998-03-06 Pembuatan n-butiraldehida dan/atau n-butanol

Country Status (11)

Country Link
US (1) US6166265A (id)
EP (1) EP0971868A1 (id)
JP (1) JP2001515499A (id)
KR (1) KR20000076304A (id)
CN (1) CN1249738A (id)
AU (1) AU6828998A (id)
BR (1) BR9808001A (id)
CA (1) CA2282538A1 (id)
DE (1) DE19710994A1 (id)
ID (1) ID22905A (id)
WO (1) WO1998041494A1 (id)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9823853D0 (en) 1998-10-30 1998-12-23 Bp Chem Int Ltd A process for making n-butyl esters from butadiene
GB9828338D0 (en) * 1998-12-22 1999-02-17 Bp Chem Int Ltd A process for making butyraldehyde from butadiene
US8962897B2 (en) 2012-12-19 2015-02-24 Celanese International Corporation Catalysts and processes for producing butanol
US9024090B2 (en) 2012-12-19 2015-05-05 Celanese International Corporation Catalysts and processes for producing butanol
US9018426B1 (en) 2013-12-19 2015-04-28 Celanese International Corporation Processes for producing multi-carbon alcohols
WO2017064064A1 (en) * 2015-10-12 2017-04-20 Basf Se Hydroformylation process for producing 1,6-disubstituted hexane derivatives
US11427518B2 (en) * 2018-03-19 2022-08-30 Saudi Arabian Oil Company Method of producing a fuel additive
CN110937745B (zh) * 2019-12-12 2022-07-12 万华化学集团股份有限公司 一种柠檬醛合成过程中高浓度废水的处理方法
CN113877635B (zh) * 2021-10-27 2024-02-06 南京延长反应技术研究院有限公司 一种铱基催化剂及其制备方法、醛化方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2922822A (en) * 1957-01-08 1960-01-26 Exxon Research Engineering Co Production of methyl butenyl ethers
DE2751766A1 (de) * 1977-11-19 1979-05-23 Basf Ag Verfahren zur isomerisierung von 3-buten-1-ol-verbindungen zu den entsprechenden 2-buten-1-ol-verbindungen
DE4400837A1 (de) * 1994-01-14 1995-07-20 Basf Ag Verfahren zur Herstellung von n-Butyraldehyd und/oder n-Butanol

Also Published As

Publication number Publication date
KR20000076304A (ko) 2000-12-26
DE19710994A1 (de) 1998-09-24
CA2282538A1 (en) 1998-09-24
BR9808001A (pt) 2000-03-08
AU6828998A (en) 1998-10-12
CN1249738A (zh) 2000-04-05
WO1998041494A1 (de) 1998-09-24
EP0971868A1 (de) 2000-01-19
JP2001515499A (ja) 2001-09-18
US6166265A (en) 2000-12-26

Similar Documents

Publication Publication Date Title
Safi et al. Palladium (0)-catalyzed substitution of allylic substrates in a two-phase aqueous-organic medium
ID22905A (id) Pembuatan n-butiraldehida dan/atau n-butanol
Price et al. Concerning the asymmetric metallation of ferrocenes by chiral lithium amide bases
Tamao et al. Silafunctional compounds in organic synthesis. 30. Intramolecular hydrosilation of alkenyl alcohols: A new approach to the regioselective synthesis of 1, 2-and 1, 3-diols
Jun et al. Directed C–C bond activation by transition metal complexes
Suginome et al. Palladium-catalyzed intramolecular cyanosilylation of alkynes leading to stereoselective synthesis of α, β-unsaturated nitriles
DK0783476T3 (da) Fremgangsmåde til fremstilling af 1,3-alkandioler og 3-hydroxyaldehyder
Brunner et al. Catalytic Hydrosilylation or Hydrogenation at One Coordination Site of [Cp′ Fe (CO)(X)] Fragments
Werner et al. Deactivation of the grubbs carbene complex [RuCl2 (CHPh)(PCy3) 2] by allylic alcohols
da Silva et al. Rhodium-catalyzed hydroformylation of allylbenzenes and propenylbenzenes: effect of phosphine and diphosphine ligands on chemo-and regioselectivity
CN101116828B (zh) 手性吡啶双噁唑啉催化剂及制备方法和应用
TW374760B (en) Preparation of n-butyraldehyde and/or n-butanol
Roucoux et al. New alkylarylamidophosphinephosphinites as chiral diphosphines for asymmetric hydrogenation of activated keto compounds
Misumi et al. Homogeneous multimetallic catalysts: Part 10. Formylation of aryl and alkenyl iodides by palladium—ruthenium bimetallic catalysts
DE60210082D1 (de) Verfahren zur herstellung von katalysatoren auf basis metallischer carbene zur hydrosilylierung von ungesättigten verbindungen und die so erhaltenen katalysatoren
Tatsumi et al. Reactions of allylic compounds such as allyl alcohols, allyl ethers, and allylamines using trans-Mo (N2) 2 (Ph2PCH2CH2PPh2) 2
MY127097A (en) Process for the carbonylation of a conjugated diene
YU30499A (sh) Endotelin intermedijari dobijeni pomoću asimetrične konjugovane adicione reakcije koristeći hiralni aditiv
Wright et al. Silylformylation of carbonyl compounds: A study of substrate, catalyst, and reaction conditions
DK0815078T3 (da) Fremgangsmåde til fremstilling af caprolactam
DE59707120D1 (de) Verfahren zur herstellung von aldehyden in anwesenheit einer rhodium und sulfonierte triarylphosphine als katalysator enthaltenden wässrigen phase
Lee et al. Regiospecific hydroesterification of vinylsilanes catalyzed by palladium-montmorillonite
TW372957B (en) Preparation of n-butyl alkyl ethers
Matsuda et al. Iridium-catalyzed crossed aldol coupling and a new concept to form an Ir–Si species
PL355526A1 (en) Method for hydroformylating olefinically unsaturated compounds