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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852648Generated: November 1, 2026

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

https://huagongshe.com/reaction/1852648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(4-Cyclohexyl-phenyl)-(3-piperazin-1-yl-azetidin-1-yl)-methanoneHCID 59626057—
Productmethyl 2,3-dihydro-1H-indole-5-carboxylateHCID 21782110—

Reaction Steps

To a solution of methyl 1H-indole-5-carboxylate 1j (2 g, 11.4 mmol) in glacial acetic acid (15 mL) at 0° C. was added sodium cyanoborohydride (1.08 g, 17.2 mmol) slowly. 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 pH of the solution was adjusted to ˜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 55a (1.79 g). MS m/z (M+H+) 178.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962607B2
Source datasetuspto-grants-2015_02
ORD IDord-bcb1e1d8f90a4c388ac9435c7fd5ac94
Source noteuspto-grants-2015_02