HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437821Generated: October 28, 2026
Sodium borohydride → HCID 22767883, compound
https://huagongshe.com/reaction/437821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22767937 | HCID 22767937 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 22767883 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04032525 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-2d88ad70b8524cd289f7bf5d36925a83 |
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| Source note | uspto-grants-1977_06 |
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