HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704610Generated: October 31, 2026
Sodium Hydroxide → HCID 15735659, compound
https://huagongshe.com/reaction/704610
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 15735543 | HCID 15735543 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15735659 | HCID 15735659 | — |
Reaction Steps
To a solution of 176 mg (0.51 millimole) of ethyl (Z)-3-cyclohexyl-2-(ethoxyisobutylphosphinoyl)methylpropenoate in 2 ml of ethanol was added 1 N sodium hydroxide (0.51 ml) and the solution was stirred at room temperature for 3 hours, and then refluxed for 30 minutes. After cooling, the reaction mixture was diluted with 30 ml of water, and extracted with 20 ml of ether. The aqueous layer was acidified with 4 N hydrochloric acid, and extracted three times with 20 ml of ether each time. The combined organic layers were washed with 10 ml of a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give 143 mg (yield of the captioned compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04988681 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-d143f3b897614f6b8c5deb4c9336a4f5 |
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| Source note | uspto-grants-1991_01 |
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