JPS54128564A - Preparation of gamma-alkyl-gamma-lactone - Google Patents

Preparation of gamma-alkyl-gamma-lactone

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Publication number
JPS54128564A
JPS54128564A JP3413478A JP3413478A JPS54128564A JP S54128564 A JPS54128564 A JP S54128564A JP 3413478 A JP3413478 A JP 3413478A JP 3413478 A JP3413478 A JP 3413478A JP S54128564 A JPS54128564 A JP S54128564A
Authority
JP
Japan
Prior art keywords
alkyl
lactone
hcl
gamma
dihalo
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
JP3413478A
Other languages
Japanese (ja)
Inventor
Hiromichi Kono
Mari Watanabe
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.)
Sagami Chemical Research Institute
Original Assignee
Sagami Chemical Research Institute
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 Sagami Chemical Research Institute filed Critical Sagami Chemical Research Institute
Priority to JP3413478A priority Critical patent/JPS54128564A/en
Publication of JPS54128564A publication Critical patent/JPS54128564A/en
Pending legal-status Critical Current

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Abstract

PURPOSE: To prepare the title compound useful as a raw material of perfumes, pharmaceuticals, pesticides, etc., and as a perfume, easily, by the dehalogenation of α-halo or α,α-dihalo-γ-alkyl-γ-lactone in the presence of Zn-HCl in acetic acid.
CONSTITUTION: An α-halo or α,α-dihalo-γ-alkyl-γ-lactone of formula I (R is alkyl; X1 is halogen; X2 is halogen, H) is dehalogenated by Zn-HCl treatment in acetic acid to afford γ-alkyl-γ-lactone of formula I. The compound I is easily prepared by the reaction of an α-olefin with di- or trichloroacetic acid ester. The equivalent ratio of Zn to the compound I is 1.5W3 to 1, and the HCl is pref. conc HCl of a concentration of ≥12N.
EFFECT: The dehalogenation reaction is selectively carried out without cleavage or reduction of the lactone ring.
COPYRIGHT: (C)1979,JPO&Japio
JP3413478A 1978-03-27 1978-03-27 Preparation of gamma-alkyl-gamma-lactone Pending JPS54128564A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3413478A JPS54128564A (en) 1978-03-27 1978-03-27 Preparation of gamma-alkyl-gamma-lactone

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3413478A JPS54128564A (en) 1978-03-27 1978-03-27 Preparation of gamma-alkyl-gamma-lactone

Publications (1)

Publication Number Publication Date
JPS54128564A true JPS54128564A (en) 1979-10-05

Family

ID=12405745

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3413478A Pending JPS54128564A (en) 1978-03-27 1978-03-27 Preparation of gamma-alkyl-gamma-lactone

Country Status (1)

Country Link
JP (1) JPS54128564A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4954623A (en) * 1989-03-20 1990-09-04 Eli Lilly And Company Recovery of difluoro sugar

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4954623A (en) * 1989-03-20 1990-09-04 Eli Lilly And Company Recovery of difluoro sugar

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