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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660612Generated: November 1, 2026

2,2,2-trichloroethyl 2-methyl-7-[N-(1-cyclopropylethoxy)carbonylphenylglycyl]amino-3-cephem-4-carboxylate → 2-methyl-7-[N-(1-cyclopropylethoxy)carbonylphenylglycyl]amino-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/1660612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-trichloroethyl 2-methyl-7-[N-(1-cyclopropylethoxy)carbonylphenylglycyl]amino-3-cephem-4-carboxylateHCID 131711251—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product2-methyl-7-[N-(1-cyclopropylethoxy)carbonylphenylglycyl]amino-3-cephem-4-carboxylic acidHCID 13171125487.6%

Reaction Steps

Zinc powder (3.0 g) was added under stirring at 5° C. to a solution of 2,2,2-trichloroethyl 2-methyl-7-[N-(1-cyclopropylethyoxy)carbonylphenylglycyl]amino-3-cephem-4-carboxylate (2.95 g) in a mixture of anhydrous dimethylformamido (12.5 ml) and acetic acid (3.75 ml), and the mixture was stirred for 1.5 hours. After the reaction, zinc powder was filtered off and washed with dimethylformamide (2 ml). The filtrate and the washings were combined, and the combined solution was extracted by pouring into a mixture of ethyl acetate (50 ml), ice-water (50 ml) and 10% hydrochloric acid (3 ml). The aqueous layer was further extracted with ethyl acetate (20 ml). The extract was combined, and then washed three times with water (20 ml) and once with a saturated sodium chloride aqueous solution and then dried over magnesium sulfate. After drying, the solvent was distilled off and the obtained residue was washed with ether and dried to give colorless crystals of 2-methyl-7-[N-(1-cyclopropylethoxy)carbonylphenylglycyl]amino-3-cephem- 4-carboxylic acid (2.01 g), mp 168° to 169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04308380
Source datasetuspto-grants-1981_12
ORD IDord-6e80b07f64b940c5a280a7fdce5acc13
Source noteuspto-grants-1981_12