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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729672Generated: October 31, 2026

Trifluoroacetic acid → HCID 86734116, compound

https://huagongshe.com/reaction/1729672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantHCID 68139873HCID 68139873—
ProductHCID 86734116HCID 8673411640%

Reaction Steps

A mixture of benzhydryl 7β-(α-tert.-butoxycarbonylamino-α-phenylacetamido)-3β-chloro-3α-methylcepham-4α-carboxylate (150 mg), trifluoroacetic acid (4 ml), and anisole (1 ml) is stirred at room temperature for 30 minutes, then evaporated in vacuo, The residue is treated with ether to remove soluble material. The insoluble material is 7β-(α-aminophenylacetamido)- 3β-chloro-3α-methylcepham-4α-carboxylic acid trifluoroacetate. The material is mixed with water (1.5 ml) and 25% Amberlite LA-1R is methyl isobutyl ketone (1.5 ml), and stirred for 2 hours to give an insoluble material which is collected by filtration. The solid is washed with water, methyl isobutyl ketone, and ethyl acetate, and dried to give 7β-(α-aminophenylacetamido)-3β-chloro-3α-methylcepham-4α-carboxylic acid (35 mg). Yield: 40%. IR: νmaxNujol 5.8, 5.7, 5.7μ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03989685
Source datasetuspto-grants-1976_11
ORD IDord-73546d419a0442ba8e5e8d9c08a96377
Source noteuspto-grants-1976_11