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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166040Generated: October 30, 2026

3-Bromothiophene → 1-butyl-alpha-(3-thienyl)-1H-benzotriazole-5-methanol

https://huagongshe.com/reaction/2166040

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromothiopheneHCID 13383—
Reactantbutyl-1H-benzotriazole-5-carboxaldehydeHCID 14990615—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product1-butyl-alpha-(3-thienyl)-1H-benzotriazole-5-methanolHCID 1499061658.9%

Reaction Steps

To a stirred and cooled (-78° C.) solution of 7.2 parts of 3-bromothiophene in 70 parts of 1,1'-oxybisethane were added 30 parts of a 1-butyllithium solution 1.6M in hexane. After stirring for 20 minutes at this low temperature, a solution of 6 parts of 1-butyl-1H-benzotriazole-5-carboxaldehyde in 1,1'-oxybisethane was added to the previous mixture. The reaction mixture was stirred for 2 hours at -78°~-'° C. The whole was poured into 200 parts of ice water and the product was extracted three times with 56 parts of 1,1'-oxybisethane. The combined extracts were dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of dichloromethane and methanol (98:2 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2,2'-oxybispropane. The product was filtered off and dried, yielding 5 parts (58.9%) of 1-butyl-α-(3-thienyl)-1H-benzotriazole-5-methanol; mp. 80° C. (int. 58).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943574
Source datasetuspto-grants-1990_07
ORD IDord-e1f17b5424a34446b5cdff468b9d9c8a
Source noteuspto-grants-1990_07