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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709141Generated: October 29, 2026

Water → 2-Amino-1-[2-(trifluoromethyl)phenyl]ethyl carbamate

https://huagongshe.com/reaction/709141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl N-{2-hydroxy-2-[2-(trifluoromethyl)phenyl]ethyl}carbamateHCID 66634961—
SolventAcetonitrileHCID 6342—
Product2-Amino-1-[2-(trifluoromethyl)phenyl]ethyl carbamateHCID 66635627—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 420 mg (1.38 mmol) of the compound of Example 36A in 100 ml of acetonitrile was cooled to −15° C., and a solution of 168 μl (1.93 mmol) of chlorosulphonyl isocyanate in 10 ml of acetonitrile was added dropwise. After 5 min, 50 ml of water were added and the reaction mixture was stirred further at 60° C. overnight. After cooling to RT, 50 ml of a saturated aqueous sodium bicarbonate solution were added. The mixture was extracted three times with ethyl acetate. The combined organic phases were dried over sodium sulphate and freed from the solvent on a rotary evaporator. The residue (321 mg, about 90% pure, 85% of theory) corresponded to the title compound and was reacted further without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09180120B2
Source datasetuspto-grants-2015_11
ORD IDord-e9f7d3ff36ba47e7ad30b8bb048632b0
Source noteuspto-grants-2015_11