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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534674Generated: October 25, 2026

Dichloromethane → N-benzyl-O-benzyl-D-serinamide

https://huagongshe.com/reaction/534674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantN-benzyl-O-benzyl-N2-Boc-D-serinamideHCID 7216909—
SolventWaterHCID 962—
ProductN-benzyl-O-benzyl-D-serinamideHCID 6708283393%

Reaction Steps

To a solution of N-benzyl-O-benzyl-N2-Boc-D-serinamide (16 g) and dichloromethane (80 mL), trifluoroacetic acid (80 mL) was added. The solution was stirred for 2 hours and the reaction was monitored for completion of reaction. The solution was concentrated under vacuum to obtain solid which was dissolved in water. The aqueous solution was basified to pH 8-10 with 5% sodium hydroxide and was extracted with ethyl acetate. The organic layer was separated and washed with a brine solution. The organic layer was concentrated under vacuum to obtain an oily residue 11 g of N-benzyl-O-benzyl-D-serinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853439B2
Source datasetuspto-grants-2014_10
ORD IDord-890a981e1f84428a901e3d86c71b343c
Source noteuspto-grants-2014_10