JPS6483050A - Optically active compound - Google Patents

Optically active compound

Info

Publication number
JPS6483050A
JPS6483050A JP62237288A JP23728887A JPS6483050A JP S6483050 A JPS6483050 A JP S6483050A JP 62237288 A JP62237288 A JP 62237288A JP 23728887 A JP23728887 A JP 23728887A JP S6483050 A JPS6483050 A JP S6483050A
Authority
JP
Japan
Prior art keywords
formula
expressed
optically active
acid chloride
liquid crystal
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
JP62237288A
Other languages
Japanese (ja)
Inventor
Masakatsu Nakatsuka
Isao Nishizawa
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP62237288A priority Critical patent/JPS6483050A/en
Publication of JPS6483050A publication Critical patent/JPS6483050A/en
Pending legal-status Critical Current

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

Abstract

NEW MATERIAL:A compound expressed by formula I (m is 4-10; * is asymmetric carbon). EXAMPLE:(S)-6-Hydroxynaphthalene-2-carboxylic acid-6'-methyl octyl ester. USE:A synthetic intermediate for optically active liquid crystal compound capable of providing extremely excellent ferroelectric liquid crystal, having wide temperature range and being photochemically and chemically stable. PREPARATION:2,6-Hydroxynaphthalene carboxylic acid expressed by formula II is benzylated and the benzylated product is converted into acid chloride derivative expressed by formula III using thionyl chloride, oxalic acid chloride, etc. then the above-mentioned acid chloride is reacted with various kind of optically active alcohols to give ester product expressed by formula IV, which is further subjected to debenzylation with hydrogen in the presence of pd/c to provide the compound expressed by formula I.
JP62237288A 1987-09-24 1987-09-24 Optically active compound Pending JPS6483050A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62237288A JPS6483050A (en) 1987-09-24 1987-09-24 Optically active compound

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62237288A JPS6483050A (en) 1987-09-24 1987-09-24 Optically active compound

Publications (1)

Publication Number Publication Date
JPS6483050A true JPS6483050A (en) 1989-03-28

Family

ID=17013156

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62237288A Pending JPS6483050A (en) 1987-09-24 1987-09-24 Optically active compound

Country Status (1)

Country Link
JP (1) JPS6483050A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0372385A2 (en) * 1988-12-08 1990-06-13 F. Hoffmann-La Roche Ag Naphthalene carboxylic acids, their preparation and application as medicaments
JP2007289916A (en) * 2006-03-31 2007-11-08 Tokyo Electric Power Co Inc:The Small extractor

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0372385A2 (en) * 1988-12-08 1990-06-13 F. Hoffmann-La Roche Ag Naphthalene carboxylic acids, their preparation and application as medicaments
JP2007289916A (en) * 2006-03-31 2007-11-08 Tokyo Electric Power Co Inc:The Small extractor

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