HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442001Generated: October 29, 2026
Sodium Hydroxide → HCID 21416160, compound
https://huagongshe.com/reaction/442001
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-[2-(1-Piperazinyl)ethyl]-2-oxazolidinone | HCID 12275545 | — |
| Reactant | HCID 21416136 | HCID 21416136 | — |
| Product | HCID 21416160 | HCID 21416160 | — |
Reaction Steps
11.6 G. of 10-chloro-8-fluoro-10,11-dihydro-3-trifluoromethyl-dibenzo[b,f]thiepin are treated with 27.8 g. of 3-[2-(1-piperazinyl)-ethyl]-2-oxazolidinone and stirred at 115°-120° C. for 10 minutes. The mixture is cooled and treated with 2N sodium hydroxide. The product separating as an oil is extracted with ether. The organic solution is washed to neutrality with water and shaken out with a dilute, aqueous methanesulfonic acid solution. The aqueous solution is made alkaline with sodium hydroxide and extracted with ether. The ether solution is washed with water, dried over magnesium sulfate and concentrated, whereby there is obtained 3-{2-[4-(8-fluoro-10,11-dihydro-3-trifluoromethyl-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl}-2-oxazolidinone as a yellow oil which is converted into the dimethanesulfonate (melting point 149°-151° C.) by the addition of methansulfonic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04044010 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-10b33774a9884fa2b96abdb5243f6400 |
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| Source note | uspto-grants-1977_08 |
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