HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935220Generated: October 26, 2026
Water → 2-(4-Benzyloxy-phenyl)-3-cyclopentyl-propionic acid
https://huagongshe.com/reaction/1935220
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(4-Benzyloxy-phenyl)-3-cyclopentyl-propionic acid methyl ester | HCID 67483155 | — |
| Solvent | Methanol tetrahydrofuran water | HCID 21892291 | — |
| Product | 2-(4-Benzyloxy-phenyl)-3-cyclopentyl-propionic acid | HCID 22467904 | 60.2% |
Reaction Steps
A solution of 2-(4-benzyloxy-phenyl)-3-cyclopentyl-propionic acid methyl ester (1.38 g, 4.08 mmol) in tetrahydrofuran/water/methanol (10.2 ml, 3:1:1) was treated with a 2N aqueous sodium hydroxide solution (3.06 mL, 6.12 mmol). The reaction was stirred at 25° C. for 16 h. At this time, an additional amount of the 2N aqueous sodium hydroxide solution (3.06 mL, 6.12 mmol) was added. The reaction was stirred at 25° C. for an additional 24 h. At this time, the reaction mixture was poured into water and extracted into methylene chloride. The layers were separated. The aqueous layer was acidified to pH=1 with a 1N aqueous hydrochloric acid solution and was then extracted with a solution of methylene chloride/methano (90/10). The combined organic extracts were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 50/50 hexanes/ethyl acetate) afforded 2-(4-benzyloxy-phenyl)-3-cyclopentyl-propionic acid (0.79 g, 60.2%) as a white solid: mp 112-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06384220B2 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-1924d089a48c493f90a77158de1f36fc |
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| Source note | uspto-grants-2002_05 |
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