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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376720Generated: November 1, 2026

Sodium borohydride → HCID 22918293, compound

https://huagongshe.com/reaction/1376720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57074874HCID 57074874—
SolventMethanolHCID 887—
ProductHCID 22918293HCID 2291829377%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-Methyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline carboxylic acid(7 g) was added to methyl alcohol(800 ml), and stirred at 0° C. After sodium borohydride(4.3 g) and p-toluene sulfonic acid(cat.amount) were added thereto, the reaction mixture was refuluxed for an hour, and the organic solvent was removed under reduced pressure. To the residue was added chloroform(500 ml), and it was washed twice with water (200 ml). The separated organic layer was dehydrated, and concentrated. The residue was solidified with pet. ether, and dried to give the bright-yellow-above-indicated compound(3.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663331
Source datasetuspto-grants-1997_09
ORD IDord-8bca7216905d437b8c71b8496913592f
Source noteuspto-grants-1997_09