Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389770Generated: October 30, 2026

N-(tert-butoxycarbonyl)-2-aminoethanethiol → HCID 20295353, compound

https://huagongshe.com/reaction/1389770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(tert-butoxycarbonyl)-2-aminoethanethiolHCID 3017761—
ReactantN-Formyl-4-bromomethylpiperidineHCID 19812293—
SolventMethanolHCID 887—
SolventPotassium HydroxideHCID 14797—
ProductHCID 20295353HCID 20295353—

Reaction Steps

To a solution of (A) (5.3 g, 0.03 mole) in methanol (10 ml), 5 N potassium hydroxide in methanol (5 ml) was added, followed by N-formyl-4-bromomethylpiperidine (5.2 g, 0.025 mole). The mixture was left at room temperature for 20 hours. After removal of the solvent in vacuo, the residue was diluted with ether (50 ml) and filtered. The filtrate was washed with two 5 ml portions of 2 N sodium hydroxide, followed by water and dried. The solvent was stripped in vacuo, and the residue was chromatographed on silica gel (100 g), eluting with ether to give (B) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04246262
Source datasetuspto-grants-1981_01
ORD IDord-567d81fe96a14c83a7c40d9c8471df5d
Source noteuspto-grants-1981_01