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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230215Generated: November 2, 2026

tert-Butyl (2S)-(adamant-1-ylmethoxycarbonylamino)-3-tert-butoxycarbonylaminopropionate → tert-Butyl (2S)-(adamant-1-ylmethoxycarbonylamino)-3-aminopropionate

https://huagongshe.com/reaction/2230215

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (2S)-(adamant-1-ylmethoxycarbonylamino)-3-tert-butoxycarbonylaminopropionateHCID 68828668—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
Producttert-Butyl (2S)-(adamant-1-ylmethoxycarbonylamino)-3-aminopropionateHCID 5391730494%

Reaction Steps

A solution of 8.7 g (19.22 mmol) of tert-butyl (S)-2-(1-adamantylmethyloxycarbonylamino)-3-tert-butoxycarbonylamino-propionate in 180 ml of trifluoroacetic acid/dichloromethane (1:1) was added after 1 min to 1.5 l of ice-cold NaHCO3 solution, the mixture was extracted three times with dichloromethane and the dichloromethane phases were then dried over sodium sulfate. After filtration and removal of the solvent in vacuo, 6.35 g (94%) of tert-butyl (S)-3-amino-2-(1-adamantylmethyloxycarbonylamino)propionate were obtained as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423712B1
Source datasetuspto-grants-2002_07
ORD IDord-ef94e7f3396c4ff9b3c5fb97c13cac94
Source noteuspto-grants-2002_07