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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372554Generated: November 3, 2026

Sodium borohydride → HCID 54298099, compound

https://huagongshe.com/reaction/372554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 54044111HCID 54044111—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 54298099HCID 54298099101.5%

Reaction Conditions

Temperature20 °C

Reaction Steps

8.8 g of sodium borohydride were added over 20 minutes at 22°-26° C to a solution of 8.8 g of the product of Step A in 8.8 ml of ethanol and 8.8 ml of water and the mixture was stirred for 1 hour at 20° C. The ethanol was evaporated and the mixture was poured into water and was extracted with methylene chloride. The organic extracts were washed with water, dried and evaporated to dryness to obtain 9 g of a mixture of the isomers of raw 7-(4-methylpiperazin-1-yl)-5-hydroxy-6,7,8,9-tetrahydro [5H] benzocycloheptene which was used as is for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04091115
Source datasetuspto-grants-1978_05
ORD IDord-09d39fb06ee749d58011b5fd81dda26b
Source noteuspto-grants-1978_05