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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825015Generated: October 31, 2026

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

https://huagongshe.com/reaction/1825015

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 numberUS07045518B2
Source datasetuspto-grants-2006_05
ORD IDord-85994f3b554c49b1a736841820b1fe66
Source noteuspto-grants-2006_05