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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657729Generated: October 31, 2026

Acetone → HCID 131710311, compound

https://huagongshe.com/reaction/1657729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium BicarbonateHCID 516892—
Reactantα-(Chlorocarbonyl)benzenemethanesulfonic acidHCID 13127332—
ReactantHCID 23620956HCID 23620956—
SolventWaterHCID 962—
ProductHCID 131710311HCID 131710311—

Reaction Steps

The α-sulfo-acylamido-3-halo-cephem compounds of the Formula I wherein Q is a sulfo group (--SO3H) are prepared by following the acylation procedures employed for the preparation of α-sulfobenzylpenicillins described by U.S. Patent No. 3,660,379 and in the J. Med. Chem., 15 (11), 11-5 (1972); ibid, p. 1108. For example, 7-amino-3-chloro-3-cephem-4-carboxylic acid is reacted with α-sulfophenylacetyl chloride in a mixture acetone and water containing an excess of sodium bicarbonate to yield 7-(α-sulfophenylacetamido)-3-chloro-3-cephem-4-carboxylic acid. Examples of α-sulfoacylamido-3-halo-cephems of the present invention are,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962227
Source datasetuspto-grants-1976_06
ORD IDord-986e4b98e21a4c60ba2f3eaf7f1894a2
Source noteuspto-grants-1976_06