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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166032Generated: October 30, 2026

Sodium borohydride → HCID 14990561, compound

https://huagongshe.com/reaction/2166032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 14990560HCID 14990560—
SolventEthanolHCID 702—
ProductHCID 14990561HCID 1499056162.5%

Reaction Steps

To a stirred solution of 17 parts of (4-fluorophenyl) [1-(1-methylethyl)-1H-benzotriazol-5-yl]methanone in 80 parts of ethanol were added 3.4 parts of sodium tetrahydroborate. After stirring for 1 hour at room temperature, the reaction mixture was neutralized to pH 7. The reaction mixture was concentrated and the product was extracted with ethyl acetate. The extract was 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, yielding 10.7 parts (62.5%) of α-(4-fluorophenyl)-1-(1-methylethyl)-1H-benzotriazole-5-methanol as a residue (int. 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943574
Source datasetuspto-grants-1990_07
ORD IDord-488be89842b74e2db449cbbae8f9921f
Source noteuspto-grants-1990_07