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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176033Generated: October 31, 2026

N-bromobutanimide → Benzyl 5-(bromomethyl)thiophene-2-carboxylate

https://huagongshe.com/reaction/2176033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 90370165HCID 90370165—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
ProductBenzyl 5-(bromomethyl)thiophene-2-carboxylateHCID 8953460362.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 5.27 g of benzyl 5-methylthiophene-2-carboxylate and 100 mL of carbon tetrachloride were added 4.18 g of N-bromosuccinimide (NBS) and 142 mg of azobisisobutyronitrile (AIBN), followed by stirring overnight at 80° C. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=7:3), thereby obtaining 4.44 g of benzyl 5-(bromomethyl)thiophene-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062032B2
Source datasetuspto-grants-2015_06
ORD IDord-da8b347f497b44869d766cffe3a42206
Source noteuspto-grants-2015_06