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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | tert-Butyl {2-hydroxy-1-[2-(trifluoromethyl)phenyl]ethyl}carbamate | HCID 59536783 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Amino-2-[2-(trifluoromethyl)phenyl]ethyl carbamate hydrochloride | HCID 68646124 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08796324B2 |
|---|
| Source dataset | uspto-grants-2014_08 |
|---|
| ORD ID | ord-68011f39fb0d41bfbd8c63cbddce3552 |
|---|
| Source note | uspto-grants-2014_08 |
|---|