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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402775Generated: November 1, 2026

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

https://huagongshe.com/reaction/2402775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl {2-hydroxy-1-[2-(trifluoromethyl)phenyl]ethyl}carbamateHCID 59536783—
SolventAcetonitrileHCID 6342—
Product2-Amino-2-[2-(trifluoromethyl)phenyl]ethyl carbamate hydrochlorideHCID 68646124—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 570 mg (1.87 mmol) of the compound from Example 62A in 100 ml of acetonitrile was cooled to −15° C. and admixed with 325 μl (3.73 mmol) of chlorosulphonyl isocyanate. After 10 min, 50 ml of water were added and the mixture was heated at 60° C. for 4 h. After cooling to RT, the solution was rendered alkaline (pH 9-10) by addition of saturated aqueous sodium hydrogen carbonate solution and extracted three times with ethyl acetate. The combined organic phases were dried over sodium sulphate and freed from the solvents on a rotary evaporator. For complete deprotection of the amino group, the residue was admixed with 15 ml of a 4M solution of hydrogen chloride in dioxane, and the mixture was stirred at RT for 5 min and the volatile components were removed on a rotary evaporator. The residue corresponded to the title compound (630 mg, quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796324B2
Source datasetuspto-grants-2014_08
ORD IDord-68011f39fb0d41bfbd8c63cbddce3552
Source noteuspto-grants-2014_08