Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636574Generated: October 25, 2026

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

https://huagongshe.com/reaction/1636574

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-adamantylmethyloxy-carbonylamino)-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 combined dichloromethane phases were then dried over sodium sulfate. After filtration and removal of the solvent in vacuo, 6.35 g (94%) of the title compound were obtained as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034238
Source datasetuspto-grants-2000_03
ORD IDord-ef6dbdf8297741e8a0698fcec6d546b9
Source noteuspto-grants-2000_03