HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21587Generated: October 26, 2026
Water → 1-Methyl-3-(1-methylethoxy)-5-(phenylmethoxy)-1H-indole-2-carboxylic acid
https://huagongshe.com/reaction/21587
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Benzyloxy-3-isopropoxy-1-methyl-1H-indole-2-carboxylic acid tert-butyl ester | HCID 10834524 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 1-Methyl-3-(1-methylethoxy)-5-(phenylmethoxy)-1H-indole-2-carboxylic acid | HCID 10569084 | 88.4% |
Reaction Steps
A suspension of 1,1-dimethylethyl 1-methyl-3(1-methylethoxy)-5-(phenylmethoxy)-1H-indole-2-carboxylate (5.6 g, 14 mmol) in 80 mL of 2-methoxyethanol is treated with a solution of 50% aqueous sodium hydroxide (5.0 g, 63 mmol) followed by the addition of 15 mL of water. The mixture is stirred at reflux for 3 hours, then cooled and added to 700 mL of water. The mixture is heated on a hot plate until nearly one phase and filtered hot. The warm filtrate is immediately treated with 50 mL of 4.0N HCl. After cooling to room temperature, followed by 1 hour in an ice bath, the precipitated solid is filtered and washed with 25% methanol in water to give 4.2 g (88%) of product suitable for further synthesis. A sample recrystallized from ethyl acetate-hexane has mp 136° C.-dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05424329 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-9619e7daf99446a5b0dceda6fd6203e7 |
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| Source note | uspto-grants-1995_06 |
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