HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248315Generated: October 27, 2026
Tetrahydrofuran → 1-butyl-1H-benzotriazole-5-methanol
https://huagongshe.com/reaction/2248315
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium aluminum hydride | HCID 28112 | — |
| Reactant | 1-Butyl-1,2,3-benzotriazole-5-carboxylic acid | HCID 10331019 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-butyl-1H-benzotriazole-5-methanol | HCID 14990570 | 42.7% |
Reaction Steps
To a stirred and cooled (0° C.) suspension of 23.1 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05039677 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-f69957a8b6054c75ae095c37b751b541 |
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| Source note | uspto-grants-1991_08 |
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