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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223243Generated: October 29, 2026

Tetrahydrofuran → HCID 12669332, compound

https://huagongshe.com/reaction/223243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 12669330HCID 12669330—
ReactantHCID 20200458HCID 20200458—
ProductHCID 12669332HCID 1266933282%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352805
Source datasetuspto-grants-1982_10
ORD IDord-24a233adc45a427ba80f3ae2e2782bd6
Source noteuspto-grants-1982_10