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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593255Generated: October 29, 2026

Trifluoroacetic acid → N-benzyl-O-benzyl-D-serinamide

https://huagongshe.com/reaction/593255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantN-benzyl-O-benzyl-N2-Boc-D-serinamideHCID 7216909—
SolventDichloromethaneHCID 6344—
ProductN-benzyl-O-benzyl-D-serinamideHCID 6708283370%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of N-benzyl-O-benzyl-N2-Boc-D-serinamide (3 g) and dichloromethane (15 mL), trifluoroacetic acid (15 mL) was added. The solution was stirred for 2 hours at 40° C. for completion of reaction. The solution was concentrated under vacuum to remove solvents and subsequently water was added. The aqueous layer was basified to pH 8-10 with 5% sodium hydroxide. The aqueous layer was extracted with ethyl acetate and the combined organic layer was washed with brine solution. Organic layer was concentrated under vacuum to obtain an oily residue solidify by n-Hexane to give 1.55 g of N-benzyl-O-benzyl-D-serinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242926B2
Source datasetuspto-grants-2016_01
ORD IDord-9961df7748da4f09b7a63590beee884b
Source noteuspto-grants-2016_01