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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534672Generated: October 25, 2026

Benzylamine → N-benzyl-O-benzyl-N2-Boc-D-serinamide

https://huagongshe.com/reaction/534672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant(R)-3-(benzyloxy)-2-((tert-butoxycarbonyl)amino)propanoic acidHCID 2733693—
Solvent4-MethylmorpholineHCID 7972—
SolventTetrahydrofuranHCID 8028—
ProductN-benzyl-O-benzyl-N2-Boc-D-serinamideHCID 721690950%

Reaction Steps

To a cooled (−20° C.) solution of N-Boc-O-benzyl-D-serine (26 g) in tetrahydrofuran (208 mL), N-methylmorpholine (15 mL) was added and reaction mixture was stirred for 5 minutes. isobutylchloformate (18 mL) was added to the reaction mixture in 5 minutes at −20° C. The solution was further stirred for 5 minutes at −20° C. and benzyl amine (15.01 mL) was added to in it in 5 minutes at −20° C. The solution was stirred for 1 hr at −20° C. The solution was allowed to warm at room temperature and stirred for 1 hour. The precipitated hydrochloride salt of N-methylmorpholine was filtered. The filtrate was concentrated under vacuum to obtain solid 17 g N-benzyl-O-benzyl-N2-Boc-D-serinamide after crystallization from diisopropylether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853439B2
Source datasetuspto-grants-2014_10
ORD IDord-237040d7a9c14971ab822c563cb0ee99
Source noteuspto-grants-2014_10