HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907887Generated: November 2, 2026
Water → Propan-2-yl 3-cyclopentyl-1-methyl-1H-indole-6-carboxylate
https://huagongshe.com/reaction/1907887
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Lithium propan-2-olate | HCID 23673350 | — |
| Reactant | 1H-Indole-6-carboxylic acid, 3-cyclopentyl-1-methyl-, methyl ester | HCID 59658510 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Propan-2-yl 3-cyclopentyl-1-methyl-1H-indole-6-carboxylate | HCID 66835544 | 95.2% |
Reaction Steps
The mixture of methyl 3-cyclopentyl-1-methyl-1H-indole-6-carboxylate (50.0 g, 0.194 mol) and lithium isopropoxide (16.2 g, 95%, 0.233 mol) in 2-propanol was stirred at 65±5° C. for at least 30 min for complete trans-esterification. The batch was cooled to 40±5° C. and water (600 g) was added at a rate to maintain the batch temperature at 40±5° C. After addition, the mixture was cooled to 20-25° C. over 2±0.5 h and held at 20-25° C. for at least 1 h. The batch was filtered and rinsed with 28 wt % 2-propanol in water (186 g), and water (500 g). The wet cake was dried in vacuo (≦200 Torr) at 40-45° C. until the water content was ≦0.5% to give isopropyl 3-cyclopentyl-1-methyl-1H-indole-6-carboxylate (52.7 g, 95% yield) in 99.2 A % (240 nm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598183B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-e9124e6e20e5438b947575858e1ce6e3 |
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| Source note | uspto-grants-2013_12 |
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