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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723105Generated: November 3, 2026

Sodium borohydride → HCID 14518421, compound

https://huagongshe.com/reaction/1723105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 14518420HCID 14518420—
SolventMethanolHCID 887—
ProductHCID 14518421HCID 1451842180%

Reaction Steps

(a-4) To a stirred solution of 3.4 parts of (1-methoxy-2-methyl-1H-benzimidazol-5-yl) phenylmethanone in 64 parts of methanol were added 0.6 parts of sodium tetrahydroborate. After stirring for 30 minutes at room temperature, the methanol layer was evaporated. Water was added to the residue and the product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was crystallized from 45 parts of ethyl acetate. The product was filtered off and dried, yielding 2.8 parts (80%) of 1-methoxy-2-methyl-α-phenyl-1H-benzimidazole-5-methanol (int. 51).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859684
Source datasetuspto-grants-1989_08
ORD IDord-82c77c54cd4f472194f5dfbbd80a87bb
Source noteuspto-grants-1989_08