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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363252Generated: October 31, 2026

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

https://huagongshe.com/reaction/363252

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 from Example 11 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 oragnic 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 numberUS05872299
Source datasetuspto-grants-1999_02
ORD IDord-9a24da3847d54743a433a02f0e9bf4d4
Source noteuspto-grants-1999_02