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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158385Generated: November 1, 2026

Water → Methyl 3-methyl-1H-indole-6-carboxylate

https://huagongshe.com/reaction/1158385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactantmethyl 3-formyl-1H-indole-6-carboxylateHCID 735867—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventDimethylformamideHCID 6228—
SolventSulfolaneHCID 31347—
ProductMethyl 3-methyl-1H-indole-6-carboxylateHCID 21938240—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-formyl-1H-indole-6-carboxylic acid methyl ester (5 g, 24.6 mmol), p-toluene-sulfonic acid (704 mg, 3.7 mmol) and p-toluenesulfonylhydrazide (5.49 g, 29.5 mmol) in a mixture of dimethylformamide (50 mL) and sulfolane (25 mL) is heated at 100° C. for 15 min. Then cooled to RT, before the addition of sodium cyanoborohydride (6.2 g, 98.4 mmol, 2 g portions after 10 min intervals). The resulting mixture is heated at 100° C. for 2 h, cooled to RT and poured into a mixture of ice and water (250 mL) leading to a white precipitate. Water (500 mL) is added, and the mixture is stirred for 30 min before filtration. The off-white solid is washed with warm water. Toluene is added and removed by rotary evaporation to afford the title compound as a yellow solid. TLC, Rf (hexane/AcOEt 4:1)=0.3. MS (LC-MS): [M+H]+=188.1. tR (HPLC, Macherey-Nagel Nucleosil C18 column, 10-100% CH3CN/H2O/5 min, 100% CH3CN/3 min, CH3CN and H2O containing 0.1% TFA, flow: 1.5 mL/min): 5.13 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807709B2
Source datasetuspto-grants-2010_10
ORD IDord-db66c2cba08d420c84ec73a40f7af56e
Source noteuspto-grants-2010_10