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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461471Generated: November 1, 2026

Epichlorohydrin → HCID 15035854, compound

https://huagongshe.com/reaction/1461471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(tert-butoxycarbonyl)-2-aminoethanethiolHCID 3017761—
SolventEthanolHCID 702—
ProductHCID 15035854HCID 15035854102.3%

Reaction Steps

N-(t-butyloxycarbonyl)-aminoethanethiol (40 g, 225 mmole) from Example 2, and epichlorohydrin (35.4 g, 383 mmole) in 300 mL of ethanol were cooled to 0° C. and treated with potassium carbonate (35.4 g). The reaction was warmed to room temperature over 90 minutes and filtered through celite. The volatiles were removed under reduced pressure to give a clear oil (62.09 g, 100% yield) D.C.I.M.S. 270(M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05075440
Source datasetuspto-grants-1991_12
ORD IDord-80c662197df04bcbaccf6213f4be7ac2
Source noteuspto-grants-1991_12