HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841271Generated: October 30, 2026
Sodium Hydroxide → HCID 12019653, compound
https://huagongshe.com/reaction/841271
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 69691911 | HCID 69691911 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12019653 | HCID 12019653 | 87.5% |
Reaction Steps
A solution of (E)-2-[3-chloro-4-(5-methyl-tetrazol-1-yl)-phenyl]-3-cycloheptyl-acrylic acid methyl ester (1.20 g, 3.2 mmol) in ethanol (15 mL) was treated with a 1N aqueous sodium hydroxide solution (6.5 mL). The solution was heated at 45-50° C. for 15 h, at which time, thin layer chromatography analysis of the reaction mixture indicated the absence of starting material. The reaction mixture was concentrated in vacuo to remove ethanol. The residue was diluted with water (50 mL) and extracted with diethyl ether (1×50 mL) to remove any neutral impurities. The aqueous layer was then acidified with a 1N aqueous hydrochloric acid solution, and the resulting acid was extracted into ethyl acetate (2×70 mL). The combined organic layers were washed with a saturated aqueous sodium chloride solution (1×50 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to afford (E)-2-[3-chloro-4-(5-methyl-tetrazol-1-yl)-phenyl]-3-cycloheptyl-acrylic acid (1.01 g, 87%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06369232B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-0ad6d86246204c71a1bb700a31f7e48d |
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| Source note | uspto-grants-2002_04 |
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