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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235097Generated: October 31, 2026

Ammonium Hydroxide → HCID 68701783, compound

https://huagongshe.com/reaction/2235097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethyl 4-methoxy-1H-indole-6-carboxylateHCID 12140116—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 68701783HCID 6870178370%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium cyanoborohydride (3.6 g, 57.8 mmol, 3 equiv.) was added to a stirred solution of 4-methoxy-1H-indole-6-carboxylic acid methyl ester (3.96 g, 19.3 mmol, 1 equiv.) in acetic acid (40 mL) at room temperature over 5 minutes. The mixture was stirred for 30 minutes, then cooled to 0° C. and slowly poured onto concentrated ammonium hydroxide (78 mL, d=0.880) at 0° C. The mixture was diluted with water (20 mL) extracted with dichloromethane (4×25 mL). The organic layers were combined, dried over Na2SO4 and the solvent was removed under vacuum. The crude mixture was purified by flash column chromatography (SiO2, dichloromethane) and the fractions combined to afford 4-methoxy-2,3-dihydro-1H-indole-6-carboxylic acid methyl ester, 2.8 g (70% yield). LC @215 nm; Rt 0.85: 97%, m/z (ES+): 208 (M+H+.); δH (400 MHz; d6-DMSO) 6.90 (1H, s), 6.86 (1H, s), 3.80 (3H, s), 3.79 (3H, s), 3.49 (2H, t), 2.89 (2H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713996B2
Source datasetuspto-grants-2010_05
ORD IDord-da585ef13b844494bec938c68e75ebd3
Source noteuspto-grants-2010_05