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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853167Generated: October 30, 2026

Trifluoroacetic acid → HCID 11687874, compound

https://huagongshe.com/reaction/853167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassio isocyanateHCID 11051572—
ReactantHCID 69039049HCID 69039049—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductHCID 11687874HCID 1168787444.3%

Reaction Steps

Under an argon atmosphere and at room temperature, a suspension of 1.0 g of 2-[4-(3-fluoro-benzyloxy)-phenyl]-ethanol and 0.66 g of potassium isocyanate in 2 ml of benzene was treated dropwise under stirring with 0.62 ml of trifluoroacetic acid. After stirring for 18 h at room temperature, the reaction mixture was diluted with water, then extracted three times with dichloromethane. The combined organic layers were dried over potassium carbonate and evaporated. There were obtained 0.52 g (44% of theory) of carbamic acid 2-[4-(3-fluoro-benzyloxy)-phenyl]-ethyl ester as a white solid; MS: m/e=290 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253318B2
Source datasetuspto-grants-2007_08
ORD IDord-709065a3f569419ab1cc3846d37a282e
Source noteuspto-grants-2007_08