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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982925Generated: October 31, 2026

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

https://huagongshe.com/reaction/982925

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 numberUS06861539B1
Source datasetuspto-grants-2005_03
ORD IDord-81d2c15a2bc541d5b75c6fd7c4919ae1
Source noteuspto-grants-2005_03