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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419292Generated: November 4, 2026

Sodium borohydride → HCID 22767883, compound

https://huagongshe.com/reaction/2419292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22767937HCID 22767937—
SolventAcetic AcidHCID 176—
ProductHCID 22767883HCID 22767883—

Reaction Steps

6.15 G. of sodium borohydride are added in small portions over a period of 15 minutes to a solution of 12.3 g. of 1-[2-fluoro-dibenzo[b,f]oxepin-10-yl]-4-methyl-piperazine in 185 ml. of glacial acetic acid with cooling in such a manner that the temperature does not exceed 25° C. The mixture is stirred for an additional 1 hour at room temperature and the acetic acid is then evaporated in vacuo. The residue is partitioned between 3-N sodium hydroxide solution and chloroform. The aqueous phase is separated and extracted again with chloroform. The chloroform extracts are washed three times with water, dried over sodium sulfate, evaporated in vacuo, and there is obtained 1-[2-fluoro-10,11-dihydro-dibenz[b,f]-oxepin-10-yl]-4-methyl-piperazine as a crystalline residue. The dihydrochloride, prepared in ethanol, melts at 240°-241° C. (with decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04105664
Source datasetuspto-grants-1978_08
ORD IDord-1cfeffdce5164ba5af86cc0ea974261c
Source noteuspto-grants-1978_08