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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166036Generated: October 27, 2026

Tetrahydrofuran → 1-butyl-1H-benzotriazole-5-methanol

https://huagongshe.com/reaction/2166036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantLithium aluminum hydrideHCID 28112—
Reactant1-Butyl-1,2,3-benzotriazole-5-carboxylic acidHCID 10331019—
SolventWaterHCID 962—
Product1-butyl-1H-benzotriazole-5-methanolHCID 1499057042.7%

Reaction Steps

To a stirred and cooled (0° C.) suspension of 23.4 parts of lithium tetrahydroaluminate in 270 parts of dry tetrahydrofuran were added portionwise 45 parts of 1-butyl-1H-benzotriazole-5-carboxylic acid. Upon complete addition, stirring was continued for 1 hour at 0° C. The reaction mixture was hydrolysed with 50 parts of water. The whole was filtered and washed with a mixture of dichloromethane and methanol (90:10 by volume). The filtrate was evaporated to dry and 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, yielding 18 parts (42.7%) of 1-butyl-1H-benzotriazole-5-methanol as an oily residue (int. 10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943574
Source datasetuspto-grants-1990_07
ORD IDord-4f5f8180b03841989e8efd4abb7f354b
Source noteuspto-grants-1990_07