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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880229Generated: October 30, 2026

Chloroacetyl chloride → (1S)-1-(4-fluorophenyl)-2-(N-benzyl-N-chloroacetylamino)ethanol

https://huagongshe.com/reaction/880229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium HydroxideHCID 14798—
Reactant(1S)-1-(4-fluorophenyl)-2-(benzylamino)ethanolHCID 15983828—
SolventDichloromethaneHCID 6344—
Product(1S)-1-(4-fluorophenyl)-2-(N-benzyl-N-chloroacetylamino)ethanolHCID 6735270790.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolve (1S)-2-(benzylamino)-1-(4-fluorophenyl)ethanol (1215 g, 4.96 mol) in 12.15 L DCM and cool the mixture to 0° C. Add NaOH (1M in H2O, 5.46 L, 5.46 mol) dropwise over 30 min. Stir the mixture vigorously for 10 min while maintaining it at 0-3° C.; then add a solution of chloroacetyl chloride (616.5 g, 5.46 mol) in 4.86 L of DCM dropwise over 1 h keeping the temperature below 6° C. Stir the mixture for 1 h at 0° C.; separate the layers; and extract the aqueous phase with DCM (1×2 L). Combine the organic layer and extracts; wash them with 10% hydrochloric acid (1.5 L), water (1.5 L) and 1M NaOH (1 L). Dry over Na2SO4 and filter. Collect the filtrate and remove the solvent under reduced pressure to provide the title compound as a colorless oil (1440 g, 90%). MS (m/z): 322 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993568B2
Source datasetuspto-grants-2015_03
ORD IDord-87c36800012b4a70928596776248f882
Source noteuspto-grants-2015_03