HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866596Generated: October 28, 2026
Sodium borohydride → HCID 54428684, compound
https://huagongshe.com/reaction/866596
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 54533726 | HCID 54533726 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 54428684 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04100173 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-64a9425b8ec04ae7840273af0df38b7b |
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| Source note | uspto-grants-1978_07 |
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