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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81159Generated: October 31, 2026

Chloroacetyl chloride → N-benzyl-2-chloro-N-((2R,3R)-2-hydroxypentan-3-yl)acetamide

https://huagongshe.com/reaction/81159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
Reactant(2R,3R)-3-(benzylamino)pentan-2-olHCID 86724514—
SolventDichloromethaneHCID 6344—
ProductN-benzyl-2-chloro-N-((2R,3R)-2-hydroxypentan-3-yl)acetamideHCID 86724513—

Reaction Conditions

Temperature-40 °C

Reaction Steps

Triethylamine (0.43 mL, 3.4 mmol) was added to a −40° C. solution of (2R,3R)-3-(benzylamino)pentan-2-ol (220 mg, 1.1 mmol) in dichloromethane (100 mL), followed by the addition of 2-chloroacetyl chloride (0.10 mL, 1.1 mmol) dropwise. The reaction mixture was stirred at −40° C. for 1 hour and then quenched with saturated NaHCO3 solution. The layers were separated, and the aqueous layer was extracted with dichloromethane (3×10 mL). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. Purification of the residue on a silica gel column (0 to 50% EtOAc/hexanes) afforded N-benzyl-2-chloro-N-((2R,3R)-2-hydroxypentan-3-yl)acetamide. MS APCl calc'd for C14H20ClNO2 [M+H]+ 270. found 270.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846657B2
Source datasetuspto-grants-2014_09
ORD IDord-6a5df74267484998a9689d2c3c05eb2b
Source noteuspto-grants-2014_09