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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904021Generated: October 26, 2026

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

https://huagongshe.com/reaction/904021

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

α-Sulfo(2,3-dihydro-5-benzofuranyl)acetyl chloride is prepared according to the general method described in J. Med. Chem., 15, 1105 (1972). α-Sulfo(2,3-dihydro-5-benzofuranyl)acetic acid 20 mmole is added slowly to a solution of diethyl ether (4 ml) and thionyl cloride (150 mmole). The mixture is stirred at room temperature until the gas evolution stops. 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 diethyl ether and 30 ml of hexane and then cooled to about -25° C. The α-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 numberUS04229575
Source datasetuspto-grants-1980_10
ORD IDord-0e28808bc4294e2ebc41f61c37ed1708
Source noteuspto-grants-1980_10