Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038439Generated: October 29, 2026

Water → methyl 2,3-dihydro-1H-indole-5-carboxylate

https://huagongshe.com/reaction/2038439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactantmethyl 1H-indole-5-carboxylateHCID 2737635—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
Productmethyl 2,3-dihydro-1H-indole-5-carboxylateHCID 2178211088.6%

Reaction Steps

To a solution of methyl 1H-indole-5-carboxylate 19a (2 g, 11.4 mmol) in glacial acetic acid (15 mL) at 0° C. was slowly added sodium cyanoborohydride (1.08 g, 17.2 mmol). The mixture was allowed to warm up and stirred at room temperature for 2 h. Water was added to the resulting mixture at 0° C., and the solution was adjusted to pH˜12 with 1N aqueous NaOH. The mixture was extracted with CH2Cl2 and the organic layer was washed with brine and dried over Na2SO4. The solution was concentrated and purified by flash column chromatography (silica gel, 15% EtOAc/heptane) to give compound 24a (1.79 g). MS m/z (M+H+) 178.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575363B2
Source datasetuspto-grants-2013_11
ORD IDord-ce14a9261f224737b77fa96a9f38d0dd
Source noteuspto-grants-2013_11