HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236090Generated: October 30, 2026
Sodium Hydroxide → HCID 131714712, compound
https://huagongshe.com/reaction/236090
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | HCID 13607941 | HCID 13607941 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131714712 | HCID 131714712 | — |
Reaction Steps
A solution of 18.90 g (0.0561 mole) of 3-[(3,4-dichlorophenyl)thio]-1-(phenylmethyl)pyrrolidine (free base) and 11.0 g (0.070 mole) of phenyl chloroformate in 800 ml of methylene chloride was stirred at room temperature for 3 hr. The methylene chloride solution was extracted first with dilute sulfuric acid followed by dilute sodium hydroxide, dried and evaporated in vacuo to give an oil. The oil was suspended in 300 ml of 48% hydrobromic acid and the mixture refluxed overnight. The reaction mixture was poured over ice and the mixture made basic with sodium hydroxide. The basic mixture was extracted with methylene chloride and the methylene chloride layer separated and dried over magnesium sulfate and evaporated in vacuo to give an oil, the free base of the title compound. The hydrochloride salt was prepared in methanol with ethereal hydrogen chloride and recrystallized from methanol diethyl ether to give a white crystalline salt. On drying under high vacuum at 80° C. the solid melted. On cooling, the melt formed a gloss, the monohydrochloride, hemihydrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04642348 |
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| Source dataset | uspto-grants-1987_02 |
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| ORD ID | ord-321263409081412288414c787e7fadee |
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| Source note | uspto-grants-1987_02 |
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