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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358530Generated: October 29, 2026

Trifluoroacetic acid → HCID 13326554, compound

https://huagongshe.com/reaction/358530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantHCID 86739607HCID 86739607—
SolventDichloromethaneHCID 6344—
ProductHCID 13326554HCID 13326554158.4%

Reaction Steps

A solution of 1.0 g (1.3 mmol) of (S)-7-[[[cyclohexyl(1-oxopropoxy)methoxy](4-phenylbutyl)phosphinyl]acetyl]-1,4-dithia-7-azaspiro[4.4]nonane-8-carboxylic acid, benzhydryl ester in 10 ml of dichloromethane was stirred, cooled in an ice-bath, treated with 0.3 ml of anisole and 1.0 ml of trifluoroacetic acid (dropwise). After 90 minutes, the solvent and bulk of excess of trifluoroacetic acid were removed on a rotary evaporator and the residue was shaken with 50 ml of ethyl acetate and 20 ml of cold water. The layers were separated (5 ml of ether was added to break up the emulsion) and the organic phase was washed with three 20 ml portions of water. After back-extracting the combined aqueous layers with 25 ml of ethyl acetate, the combined organic layers were washed with 20 ml of saturated sodium chloride, dried (MgSO4), and the solvent evaporated to yield 1.26 g of a syrup. The syrup was purified by chromatography on 60 g of silica gel (60-200 mesh, d=0.37 g/ml) using 40:1:1 dichloromethane:methanol:acetic acid to give 0.74 g of a foam-like solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04468519
Source datasetuspto-grants-1984_08
ORD IDord-4e4563235f9148ae971d705604a97851
Source noteuspto-grants-1984_08