Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862474Generated: November 1, 2026

Trichloroacetyl isocyanate → HCID 514447, compound

https://huagongshe.com/reaction/1862474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl isocyanateHCID 76400—
ReactantHCID 10203491HCID 10203491—
SolventDichloromethaneHCID 6344—
ProductHCID 514447HCID 51444742.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 120 mg of 5-(3,5-Dichlorophenylthio)-1-isopropyl-4-[(4-pyridyl)methoxymethyl]-1H-pyrazole-3-methanol in 1 ml of dichloromethane at 0° C. was added 11 mg of trichloroacetyl isocyanate. The mixture was stirred for 2 h at 0° C. then the solvent was removed. The residue was dissolved in 2 ml of methanol and 1 ml of water, 100 mg of potassium carbonate added, and the mixture stirred at room temperature for 1 h. The mixture was partitioned between ethyl acetate and water. The combined extracts were dried over magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography using methanol/dichloromethane for the elution to give 12 mg of carbamic acid [5-(3,5-dichlorophenylthio)-1-isopropyl-4-[(4-pyridyl)methoxymethyl]-1H-pyrazol-3-yl]methyl ester as a white solid. Mass spectrum (ES) m/z 481 [M]+. 1H NMR (DMSO-d6) 1.25 (d, 6H), 4.50 (s, 2H), 4.52 (s, 2H), 4.80 (m, 1H), 5.05 (s, 2H), 6.55 (br s, 1H), 6.75 (br s, 1H), 7.08 (m, 2H), 7.16 (d, 2H) 7.45 (m, 1H), 8.43 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06538015B1
Source datasetuspto-grants-2003_03
ORD IDord-fdf2c0f8008345b78439f09718fa173a
Source noteuspto-grants-2003_03