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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252472Generated: November 2, 2026

Oxalyl chloride → 2-(5-t-Butylfuran-2-yl)-cyclopropanecarbonyl chloride

https://huagongshe.com/reaction/1252472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-(5-t-Butylfuran-2-yl)-cyclopropanecarboxylic acidHCID 20139962—
SolventHexaneHCID 8058—
Product2-(5-t-Butylfuran-2-yl)-cyclopropanecarbonyl chlorideHCID 20139947101.2%

Reaction Steps

A mixture of 2-(5-t-butylfuran-2-yl)-cyclopropanecarboxylic acid (3.6 g, 0.017 mol) and oxalyl chloride (4.4 g, 0.035 mol) in hexane (40 ml) was stirred at room temperature for 2 hours and then warmed at 60° C. for 3 hours. The hexane and excess oxalyl chloride were removed in vacuo to give 2-(5-t-butylfuran-2-yl)-cyclopropanecarbonyl chloride (3.9 g, 100%) as a pale yellow liquid which was used in the next stage without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04743602
Source datasetuspto-grants-1988_05
ORD IDord-d08a45b09c16472e88b16f654b30e951
Source noteuspto-grants-1988_05