JPH0240355A - Benzylalkylthiophenyl ether compound - Google Patents

Benzylalkylthiophenyl ether compound

Info

Publication number
JPH0240355A
JPH0240355A JP18780588A JP18780588A JPH0240355A JP H0240355 A JPH0240355 A JP H0240355A JP 18780588 A JP18780588 A JP 18780588A JP 18780588 A JP18780588 A JP 18780588A JP H0240355 A JPH0240355 A JP H0240355A
Authority
JP
Japan
Prior art keywords
ether
benzylalkylthiophenyl
ether compound
alkoxybenzyl
methoxybenzyl
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
JP18780588A
Other languages
Japanese (ja)
Inventor
Naoto Yanagihara
直人 柳原
Naotaka Wachi
直孝 和地
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fujifilm Holdings Corp
Original Assignee
Fuji Photo Film Co Ltd
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 Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd
Priority to JP18780588A priority Critical patent/JPH0240355A/en
Publication of JPH0240355A publication Critical patent/JPH0240355A/en
Pending legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

NEW MATERIAL:(4-Alkoxybenzyl)-4-alkylthiophenyl ether. EXAMPLE:(4-Methoxybenzyl)-4-methylthiophenyl ether. USE:A thermally meltable substance for recording material. PREPARATION:The subject compound can be produced by reacting the corresponding p-alkoxybenzyl halide with an alkylthiophenol in the presence of a basic catalyst (e.g., potassium carbonate). The reaction may be carried out in a solvent.

Description

【発明の詳細な説明】 ”(発明の″分野) 本発明は新規なベンジルアルキルチオフェニルエーテル
化合物に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to novel benzylalkylthiophenyl ether compounds.

(従来技術) 記録材料用熱可融性物質としてエーテル系化合物、チオ
エーテル系化合物は、各種知られているが、何れも発色
濃度、感度等の点でいくつかの欠点を有していた。
(Prior Art) Various ether compounds and thioether compounds are known as thermofusible substances for recording materials, but all of them have several drawbacks in terms of color density, sensitivity, and the like.

(発明の目的) 本発明の目的は記録材料用の熱可融性物質として有用な
新規なベンジルアルキルチオフェニルエーテル化合物を
提供することである。
OBJECTS OF THE INVENTION It is an object of the present invention to provide novel benzylalkylthiophenyl ether compounds useful as thermofusible substances for recording materials.

(発明の構成) 本発明は(4−アルコキシベンジル)−4−アルキルチ
オフェニルエーテルから構成される9本発明で言うアル
コキシ基、アルキルチオ基はメトキシ基、エトキシ基、
メチルチオ基、エチルチオ基を言う。
(Structure of the Invention) The present invention consists of (4-alkoxybenzyl)-4-alkylthiophenyl ether;
Refers to methylthio group and ethylthio group.

本発明の(4−アルコキシベンジ/リー4−アルキルチ
オフェニルエーテルの具体例を示す。
Specific examples of (4-alkoxybendi/4-alkylthiophenyl ether) of the present invention are shown below.

(4−メトキシベンジル)−4+、メチルチオフ”エニ
ルエーテル、(4−メトキシベンジル)−4−エチルチ
オフェニルエーテル、(4−エトキシペンジノv)−4
−メチルチオフェニルエーテル、(4−エトキシベンジ
ル)−4−エチルチオフェニルエーテル。
(4-methoxybenzyl)-4+, methylthiophenyl ether, (4-methoxybenzyl)-4-ethylthiophenyl ether, (4-ethoxypendinov)-4
-Methylthiophenyl ether, (4-ethoxybenzyl)-4-ethylthiophenyl ether.

本発明の化合物は様々な合成方法があるが、対応するp
−アルコキシベンジルハライドとアルキルチオフェノー
ルを塩基性触媒下に反応させる方法が最も簡便である。
The compounds of the present invention can be synthesized by various methods, but the corresponding p
The simplest method is to react an alkoxybenzyl halide with an alkylthiophenol under a basic catalyst.

塩基性触媒としてはアルカリ金属化合物が一般的であり
す) IJウム化合物、又はカリウム化合物等が好まし
い。
As the basic catalyst, an alkali metal compound is generally used, but an IJium compound or a potassium compound is preferable.

また反応に際しては、溶媒を使用しても差し支えない。Furthermore, a solvent may be used during the reaction.

(実施例) p−メチルチオフェノール140g及び炭酸カリウム2
(17gのN、N、  ジメチルアセトアミド11溶液
にp−メトキシベンジルクロリド160gを加え1反応
混度、85’Cで3時間攪拌しながら反応させた0反応
混合物を水にあけ、析出した結晶を濾取した後、メタノ
ール−酢酸エチルから再結晶し、(4−メトキシベンジ
ル)−4−メチルチオフェニルエーテルヲ229 g%
だ、  m、  p。
(Example) 140 g of p-methylthiophenol and 2 potassium carbonate
(160 g of p-methoxybenzyl chloride was added to 17 g of N, N, dimethylacetamide 11 solution and reacted at 85'C for 3 hours with stirring. The reaction mixture was poured into water and the precipitated crystals were filtered. After that, it was recrystallized from methanol-ethyl acetate to obtain 229 g% of (4-methoxybenzyl)-4-methylthiophenyl ether.
Da, m, p.

100.5〜101’C (実施例2〜4) 同様にして以下の化合物を得た。100.5~101'C (Examples 2 to 4) The following compounds were obtained in the same manner.

Claims (1)

【特許請求の範囲】[Claims] (4−アルコキシベンジル)−4−アルキルチオフェニ
ルエーテル
(4-alkoxybenzyl)-4-alkylthiophenyl ether
JP18780588A 1988-07-27 1988-07-27 Benzylalkylthiophenyl ether compound Pending JPH0240355A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18780588A JPH0240355A (en) 1988-07-27 1988-07-27 Benzylalkylthiophenyl ether compound

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18780588A JPH0240355A (en) 1988-07-27 1988-07-27 Benzylalkylthiophenyl ether compound

Publications (1)

Publication Number Publication Date
JPH0240355A true JPH0240355A (en) 1990-02-09

Family

ID=16212550

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18780588A Pending JPH0240355A (en) 1988-07-27 1988-07-27 Benzylalkylthiophenyl ether compound

Country Status (1)

Country Link
JP (1) JPH0240355A (en)

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