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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024482Generated: October 28, 2026

Sodium borohydride → 3-Chloro-1-(2-thienyl)-1-propanol

https://huagongshe.com/reaction/1024482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Chloro-1-(2-thienyl)-1-propanoneHCID 7567855—
SolventEthanolHCID 702—
Product3-Chloro-1-(2-thienyl)-1-propanolHCID 11658374—

Reaction Steps

For example, a method is known wherein 1-(2-thienyl)-3-chloropropan-1-one is reduced using sodium borohydride in ethanol to obtain 3-chloro-1-(2-thienyl)-1-propanol, halogen exchange is subsequently conducted in acetone using sodium iodide to obtain 3-iodo-1-(2-thienyl)-1-propanol, and then this is reacted with a monomethylamine aqueous solution in tetrahydrofuran (CHIRALITY, 12, 26-29 (2000)). However, since the raw material used in this method is 1-(2-thienyl)-3-chloropropan-1-one, which is a very unstable compound, this method is not industrially applicable.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722906B2
Source datasetuspto-grants-2014_05
ORD IDord-4468c15f9511432f9b12f9e957049382
Source noteuspto-grants-2014_05