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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620376Generated: November 1, 2026

1,5-Dibromopentane → methyl(S)-3-tert-butoxycarbonylamino-2-piperidin-1-ylpropanoate

https://huagongshe.com/reaction/1620376

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-DibromopentaneHCID 8100—
ReactantTriethylamineHCID 8471—
Reactantmethyl (2S)-2-amino-3-{[(tert-butoxy)carbonyl]amino}propanoate hydrochlorideHCID 18334328—
Solventtert-ButanolHCID 6386—
Productmethyl(S)-3-tert-butoxycarbonylamino-2-piperidin-1-ylpropanoateHCID 6705633559.7%

Reaction Conditions

Temperature40 °C

Reaction Steps

14.4 ml (104 mmol) of triethylamine are added to a solution of 8.0 g (31 mmol) of commercial methyl (S)-2-amino-3-tert-butoxycarbonylaminopropanoate hydrochloride in 160 ml of tert-butanol, and then the reaction medium is stirred for 30 min at 40° C., and filtered in order to remove the triethylammonium salts. 6 ml (44 mmol) of 1,5-dibromopentane are added to the filtrate thus obtained, and the reaction medium is heated at 80° C. for 3 days. After the insoluble material has been filtered off, the filtrate is concentrated under vacuum. The crude residue is purified by chromatography on silica gel, elution being carried out with a 70/30 heptane/ethyl acetate mixture. 5.3 g (59%) of methyl(S)-3-tert-butoxycarbonylamino-2-piperidin-1-ylpropanoate are obtained in the form of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772478B2
Source datasetuspto-grants-2014_07
ORD IDord-3ae1e6cb501e411887a921d4cbe7afb6
Source noteuspto-grants-2014_07