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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934773Generated: November 1, 2026

Trifluoroacetic acid → HCID 22467120, compound

https://huagongshe.com/reaction/1934773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 22467148HCID 22467148—
SolventDichloromethaneHCID 6344—
ProductHCID 22467120HCID 2246712050.1%

Reaction Steps

In 56 ml of methylene chloride was dissolved 18.50 g of tert-butyl 2-(2-ethoxy-2-oxoethyl)-3-oxo-4-phenethyl-1-thia-4,8-diazaspiro[4.5]decane-8-carboxylate. After adding 56 ml of trifluoroacetic acid at 0-5° C., the resulting mixture was stirred at the same temperature as above for 30 minutes and then at ambient temperature for 5 hours. The solvent was distilled off under reduced pressure, the residue was poured into a mixture of ice water and ethyl acetate, pH was adjusted to 8.0 with saturated aqueous solution of sodium hydrogen carbonate, and the organic layer was separated. The organic layer was washed successively with water and saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. Thus, 7.26 g of ethyl 2-(3-oxo-4-phenethyl-1-thia-4,8-diazaspiro[4.5]decan-2-yl)-acetate was obtained as a yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384065B1
Source datasetuspto-grants-2002_05
ORD IDord-47dbaefbd30a4da8934c46bef56e4084
Source noteuspto-grants-2002_05