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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium propan-2-olateHCID 23673350—
Reactant1H-​Indole-​6-​carboxylic acid, 3-​cyclopentyl-​1-​methyl-​, methyl esterHCID 59658510—
SolventIsopropanolHCID 3776—
ProductPropan-2-yl 3-cyclopentyl-1-methyl-1H-indole-6-carboxylateHCID 6683554495.2%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598183B2
Source datasetuspto-grants-2013_12
ORD IDord-e9124e6e20e5438b947575858e1ce6e3
Source noteuspto-grants-2013_12