Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724875Generated: October 30, 2026

Water → N-benzyl-N-(tert-butoxycarbonyl)-L-phenylalaninal

https://huagongshe.com/reaction/724875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantN-(t-Butoxycarbonyl)-N-benzyl-L-phenylalaninolHCID 15434535—
SolventDimethyl SulfoxideHCID 679—
ProductN-benzyl-N-(tert-butoxycarbonyl)-L-phenylalaninalHCID 11099858100%

Reaction Steps

To a solution of 2.38 g (6.98 mmoles) of N-(t-butoxycarbonyl)-N-benzyl-L-phenylalaninol in 3.8 mL (27.2 mmoles) of triethylamine at 10° C. was added a solution of 4.33 g (27.2 mmoles) of sulfur trioxide pyridine complex in 17 mL of dimethyl sulfoxide. The mixture was warmed to room temperature and stirred for one hour. Water (16 mL) was added and the mixture was extracted with 20 mL of ethyl acetate. The organic layer was washed with 20 mL of 5% citric acid, 20 mL of water, 20 mL of brine, dried over magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to give 2.37 g (100% yield) of N-(t-Butoxycarbonyl)-N-benzyl-L-phenylalaninal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705500
Source datasetuspto-grants-1998_01
ORD IDord-48d6e0ef9cb548c3b92a7d1d7828bca9
Source noteuspto-grants-1998_01