HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416970Generated: October 31, 2026
Sodium Hydroxide → 4-[3-[6-(3-Bromo-5-methoxymethyl-phenoxy)-hexyl]-2-(2-carboxy-ethyl)-phenoxy]-butyric acid
https://huagongshe.com/reaction/416970
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-[3-[6-(3-Bromo-5-methoxymethyl-phenoxy)-hexyl]-2-(2-ethoxycarbonyl-ethyl)-phenoxy]-butyric acid ethyl ester | HCID 59496804 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-[3-[6-(3-Bromo-5-methoxymethyl-phenoxy)-hexyl]-2-(2-carboxy-ethyl)-phenoxy]-butyric acid | HCID 59496791 | 89% |
Reaction Steps
To a solution of 4-[3-[6-(3-Bromo-5-methoxymethyl-phenoxy)-hexyl]-2-(2-ethoxycarbonyl-ethyl)-phenoxy]-butyric acid ethyl ester (500 mg, 0.82 mmol) in hot ethanol (20 mL) was added aqueous 2.0 N sodium hydroxide (5 mL). The resulting solution was heated to 60° C. and stirred for 4 h. Then, the reaction mixture was cooled down and diluted with EtOAc, washed with 10% aq. HCl and brine. The combined ethyl acetate extracts were dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure to afford 400 mg (89%) of title compound as a light yellow oil. HR-ES(+) calcd for C27H35O7Br [M+Na]+ 573.1458, observed 573.1459.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088936B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-c96e9fa1dd5f4f049b06362384a4ef6d |
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| Source note | uspto-grants-2012_01 |
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