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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679629Generated: October 31, 2026

Phenylacetyl chloride → HCID 178431926, compound

https://huagongshe.com/reaction/1679629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantSodium HydroxideHCID 14798—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant6(Triphenylmethylamino)-2,2-dimethyl-3-(5-tetrazolyl)penamHCID 178431921—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventDiisopropyl EtherHCID 7914—
ProductHCID 178431926HCID 178431926—

Reaction Steps

A mixture of p-toluenesulfonic acid monohydrate (788 mg., 4.14 mmoles), acetone (35 ml.) and 6-triphenylmethylamino-2,2-dimethyl-3-(5-tetrazolyl)penam (2.0 g.,) 4.14 mmoles) is stirred for twenty minutes at room temperature and is then diluted with water (100 ml.) and isopropylether (100 ml.). The biphasic mixture is stirred vigorously and adjusted to pH 7 with 2N sodium hydroxide. Phenylacetyl chloride (700 mg., 4.55 mmoles freshly distilled) is added and the reaction mixture maintained at pH between 5.5-6.5 by addition of 2N sodium hydroxide as necessary. Reaction is continued until the pH levels off at 6.5. The two phases are separated and the aqueous phase washed with ether (2 × 50 ml.). It is then layered with chloroform (100 ml.) and adjusted to pH 2 by addition of 6N HCl. The mixture is stirred, the phases separated and the aqueous phase extracted with chloroform (2 × 50 ml.). The chloroform phases are combined, dried (Na 2 SO4), and then concentrated under reduced pressure to about 50 ml. volume. A 1:1 solution of ether-hexane is added dropwise with vigorous stirring to the concentrate until precipitation of the product is complete. The white precipitate is filtered and air-dried. Yield = 850 mg. (57.4%) m.p. 168°-170°;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04081455
Source datasetuspto-grants-1978_03
ORD IDord-fa26a81615664120aaa8598d3f300e07
Source noteuspto-grants-1978_03