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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866596Generated: October 28, 2026

Sodium borohydride → HCID 54428684, compound

https://huagongshe.com/reaction/866596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 54533726HCID 54533726—
SolventAcetic AcidHCID 176—
ProductHCID 54428684HCID 54428684—

Reaction Steps

48.6 G. of 4-[2,8-dimethyl-dibenz[b,f]oxepin-10-yl]-1-piperazinecarboxylic acid ethyl ester are dissolved in 750 ml. of glacial acetic acid. 18.9 G. of sodium borohydride are added in small portions within 20 minutes with stirring and cooling in such a manner that the temperature does not exceed 25° C. The mixture is stirred for an additional 30 minutes at 25° C. and then the glacial acetic acid is removed by distillation in vacuo. The residue is partitioned between chloroform and aqueous sodium hydroxide solution. The organic phase is separated and washed with water. The aqueous phases are extracted two additional times with chloroform. The combined chloroform extracts are dried over sodium sulfate, evaporated in vacuo, and there is obtained crude 4-[10,11-dihydro-2,8-dimethyl-dibenz[b,f]oxepin-10-yl]-1-piperazinecarboxylic acid ethyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04100173
Source datasetuspto-grants-1978_07
ORD IDord-64a9425b8ec04ae7840273af0df38b7b
Source noteuspto-grants-1978_07