HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249439Generated: October 29, 2026
Hydrochloric Acid → HCID 45261624, compound
https://huagongshe.com/reaction/249439
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 10694749 | HCID 10694749 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 45261624 | HCID 45261624 | 24% |
Reaction Steps
E or Z-(R)-1-[2-[[2-(3-Fluorophenyl)-2-(2-methylphenyl)-ethenyl] oxy]ethyl]-3-piperidine carboxylic acid ethyl ester (0.40 g, 0.00097 mol) (prepared as described in Method A) was dissolved in ethanol (5 ml) and 12 N sodium hydroxide solution (0.3 ml) was introduced. After stirring the solution at room temperature for 5 h, 37% hydrochloric acid solution was added until the pH was measured as ca. 1. Dichloromethane (250 ml) was introduced, and the resultant precipitate was dissolved by addition of ice portionwise with vigorous stirring. The organic phase was separated, dried (Na ) and evaporated to a residue, which was co-evaporated with acetone. Recrystallization from acetone provided the title compound (0.10 g, 24%) as a white solid, m.p. 193°-195°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05214057 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-93c820249a0b4c069698baeda451fa6b |
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| Source note | uspto-grants-1993_05 |
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