HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276196Generated: October 30, 2026
Potassium Hydroxide → HCID 53348310, compound
https://huagongshe.com/reaction/276196
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 53654715 | HCID 53654715 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53348310 | HCID 53348310 | — |
Reaction Steps
A solution of the isomeric mixture of 2-(3-chloro-4-methanesulfonyl-phenyl)-3-cyclopentyl-acrylic acid ethyl ester [500 mg, 1.40 mmol, (E):(Z)=2:1] in ethanol (16 mL) was treated with a solution of potassium hydroxide (393.6 mg, 7.00 mmol) in water (3.7 mL). The yellow solution was stirred for 3 h at 25° C. and then concentrated in vacuo to remove the ethanol. The remaining aqueous layer was acidified to pH=2 with a 1N aqueous hydrochloric acid solution and then extracted with methylene chloride (3×15 mL). The combined organic layers were then dried over sodium sulfate, filtered and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 75/25 hexanes/ethyl acetate plus 1% acetic acid) afforded (E)-2-(3-chloro-4-methanesulfonyl-phenyl)-3-cyclopentyl-acrylic acid (458 mg, 99%, 95% is the E isomer) as a white foam: FAB-HRMS m/e calcd for C15H17ClO4S (M+H)+329.0614, found 329.0628.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06353111B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-31c5c49fe3c44ec8ae16bb0cd2153988 |
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| Source note | uspto-grants-2002_03 |
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