JPS55113774A - Production of bis(5-substituted-2-furyl)methane derivative - Google Patents

Production of bis(5-substituted-2-furyl)methane derivative

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Publication number
JPS55113774A
JPS55113774A JP2038379A JP2038379A JPS55113774A JP S55113774 A JPS55113774 A JP S55113774A JP 2038379 A JP2038379 A JP 2038379A JP 2038379 A JP2038379 A JP 2038379A JP S55113774 A JPS55113774 A JP S55113774A
Authority
JP
Japan
Prior art keywords
compound
formula
substituted
acid
furyl
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
JP2038379A
Other languages
Japanese (ja)
Inventor
Kenji Saito
Hiroshi Yamachika
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP2038379A priority Critical patent/JPS55113774A/en
Publication of JPS55113774A publication Critical patent/JPS55113774A/en
Pending legal-status Critical Current

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Abstract

PURPOSE: The mutual reaction of (5-substituted-2-furyl)hydroxymethane derivative is conducted in the presence of an acid in water and/or an inert organic solvent to produce title compound used as intermediate of medicines and agricultural chemicals.
CONSTITUTION: The mutual reaction of a compound of formula I (R, R' are 1W5C alkyl, 3W5C alkenyl with a double bond on the terminal) is carried out in the presence of an acid, e.g., hydrochloric acid, in water or an inert organic solvent, e.g., dioxane, or their mixture, usually at 10W100°C, preferably 30W80°C to give the objective compound of formula II in a very short time with no complicated operations in high yield. The compound of formula I is obtained by, e.g., reaction of a 5-substituted furfural with a Grignard reagent in high yield. The amount of the acid used is 1W500pts.wt. per 1000 parts of the compound of formula I.
COPYRIGHT: (C)1980,JPO&Japio
JP2038379A 1979-02-22 1979-02-22 Production of bis(5-substituted-2-furyl)methane derivative Pending JPS55113774A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2038379A JPS55113774A (en) 1979-02-22 1979-02-22 Production of bis(5-substituted-2-furyl)methane derivative

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2038379A JPS55113774A (en) 1979-02-22 1979-02-22 Production of bis(5-substituted-2-furyl)methane derivative

Publications (1)

Publication Number Publication Date
JPS55113774A true JPS55113774A (en) 1980-09-02

Family

ID=12025506

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2038379A Pending JPS55113774A (en) 1979-02-22 1979-02-22 Production of bis(5-substituted-2-furyl)methane derivative

Country Status (1)

Country Link
JP (1) JPS55113774A (en)

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