HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658744Generated: October 30, 2026
Water → 1-(8-Fluoro-2-methyl-dibenzo[b,f]thiepin-10-yl)-4-methyl-piperazine
https://huagongshe.com/reaction/1658744
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 8-fluoro-2-methyl-dibenzo[b,f]thiepin-10(11H)-one | HCID 12275541 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-(8-Fluoro-2-methyl-dibenzo[b,f]thiepin-10-yl)-4-methyl-piperazine | HCID 21449875 | — |
Reaction Steps
18 g of 8-fluoro-2-methyl-dibenzo[b,f]thiepin-10(11H)-one in 140 ml of absolute benzene are together with 33.2 ml of N methylpiperazine within 1/2 hour at 20°-25° treated with a solution of 5.8 ml of titanium tetrachloride in 40 ml of absolute benzene. The reaction mixture is subsequently heated for 20 hours under reflux conditions. The reaction mixture is poured, with vigorous stirring, into a mixture of 40 ml of saturated aqueous sodium bicarbonate solution and 120 ml of water, subsequently filtered and extracted with chloroform. The organic phase is dried and evaporated. One obtains 1-(8-fluoro-2-methyl-dibenzo[b,f]thiepin-10-yl)-4-methyl-piperazine, which is converted into the corresponding maleate by treatment with maleic acid. The maleate melts at 244° with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03966737 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-2bff0885b2434bb9b785c03d3cf03436 |
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| Source note | uspto-grants-1976_06 |
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