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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466019Generated: November 1, 2026

Chloroacetyl chloride → HCID 131732669, compound

https://huagongshe.com/reaction/1466019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantHCID 121005435HCID 121005435—
SolventDichloromethaneHCID 6344—
ProductHCID 131732669HCID 131732669—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of tert-Butyl (2-{[2-(3-cyano-4-fluorophenyl)ethyl]amino}ethyl)carbamate (0.9 g, 3.1 mmol) and TEA (0.4 g, 3.7 mmol) in 10 mL of anhydrous DCM was added chloroacetyl chloride (0.4 g, 3.7 mmol) dropwise at 0° C. The mixture was stirred at 0° C. for 1 h, and then the solvent was evaporated. The residue was partitioned between EtOAc and water. The organic layer was dried and evaporated. The residue was purified with prep-TLC to give tert-Butyl (2-{(chloroacetyl) [2-(3-cyano-4-fluorophenyl)ethyl]amino}ethyl)carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999990B2
Source datasetuspto-grants-2015_04
ORD IDord-767c2f2f618045ec889f2d35dda51c08
Source noteuspto-grants-2015_04