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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651643Generated: November 2, 2026

N-bromobutanimide → 2-(2-Bromothiophen-3-yl)ethan-1-ol

https://huagongshe.com/reaction/1651643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantThiophene-3-ethanolHCID 83731—
SolventCarbon TetrachlorideHCID 5943—
Product2-(2-Bromothiophen-3-yl)ethan-1-olHCID 1935957299.5%

Reaction Steps

To a stirred solution of 2-(3-thienyl)ethanol (25.0 g, 0.195 mol) in carbon tetrachloride (250 ml) was added N-bromosuccinimide (34.7 g, 0.195 mol) in several portions over a 15 minute period. The mixture was stirred at room temperature for one hour. The succinimide was removed by filtration and the filtrate was concentrated in vacuo at room temperature to give the product as a viscous amber oil (40.2 g) (99%). TLC indicated that the product was pure and mass spectral analysis showed a molecular ion at M/Z 206. NMR supported the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929637
Source datasetuspto-grants-1990_05
ORD IDord-05da1af5a8bd4188b994e3da1f921a0e
Source noteuspto-grants-1990_05