HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223243Generated: October 29, 2026
Tetrahydrofuran → HCID 12669332, compound
https://huagongshe.com/reaction/223243
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 12669330 | HCID 12669330 | — |
| Reactant | HCID 20200458 | HCID 20200458 | — |
| Product | HCID 12669332 | HCID 12669332 | 82% |
Reaction Steps
A mixture of 0.50 g (1.07 mmoles) of [2-[(1,3,4,5-tetrahydro-7,8-dimethoxy-2-benzoxepin-1-yl)methoxy]ethyl]-4-nitrobenzenesulfonate, 0.22 g (1.07 mmoles) of o-methoxyphenylpiperazine, 0.15 ml (1.07 mmoles) of triethylamine, and 20 ml of tetrahydrofuran is stirred at room temperature for 24 hours. After removing the tetrahydrofuran in vacuo, the reaction mixture is extracted with methylene chloride and aqueous sodium bicarbonate. The organic layer is filtered through sodium sulfate, taken to dryness, and chromatographed on silica gel using 3% methanol methylene chloride eluent to give 0.40 g (82%) of 1-[2-[(1,3,4,5-tetrahydro-7,8-dimethoxy-2-benzoxepin-1-yl)methoxy]ethyl]-4-(2-methoxyphenyl)piperazine. The dihydrochloride salt was prepared with hydrochloric acid in ethyl ether, m.p. 172°-175°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04352805 |
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| Source dataset | uspto-grants-1982_10 |
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| ORD ID | ord-24a233adc45a427ba80f3ae2e2782bd6 |
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| Source note | uspto-grants-1982_10 |
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