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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390218Generated: October 27, 2026

Dimethylformamide → Sulfo(2,3-dihydro-5-benzofuranyl)acetyl chloride

https://huagongshe.com/reaction/1390218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
ReactantSulfo(2,3-dihydro-5-benzofuranyl)acetic acidHCID 23335828—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductSulfo(2,3-dihydro-5-benzofuranyl)acetyl chlorideHCID 23335837—

Reaction Steps

Sulfo(2,3-dihydro-5-benzofuranyl)acetyl chloride is prepared according to the general procedure described in J. Med. Chem., 15, 1105 (1972). Sulfo(2,3-dihydro-5-benzofuranyl)acetic acid (20 mmole) is added slowly to a solution of ether (4 ml) and thionyl chloride (150 mmole). The mixture is stirred at room temperature until the gas evolution stopped. Then about 0.2 ml of dimethylformamide is added and the solution heated at 40° C. for 4 hours. The mixture is diluted with 30 ml of ether and 30 ml of hexane and then cooled to -25° C. Sulfo(2,3-dihydro-5-benzofuranyl)acetyl chloride is recovered from the mixture and used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04138397
Source datasetuspto-grants-1979_02
ORD IDord-6ece8161c25f42f381ae84e7369f6b79
Source noteuspto-grants-1979_02