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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489113Generated: October 28, 2026

Cesium carbonate → 2-[(1-Benzyl-2-ethyl-6,7,8,9-tetrahydro-1h-benz[g]indol-4-yl)oxy]acetic acid methyl ester

https://huagongshe.com/reaction/489113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBoron tribromideHCID 25134—
ReactantMethyl bromoacetateHCID 60984—
Reactant1-Benzyl-2-ethyl-4-methoxy-6,7,8,9-tetrahydro-1h-benz[g]indoleHCID 11336164—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-[(1-Benzyl-2-ethyl-6,7,8,9-tetrahydro-1h-benz[g]indol-4-yl)oxy]acetic acid methyl esterHCID 1131491463.4%

Reaction Steps

A solution of 1-benzyl-2-ethyl-4-methoxy-6,7,8,9-tetrahydro-1H-benz[g]indole (660 mg, 2.07 mmol) in methylene chloride (10 mL) was cooled to 0° C. and treated with boron tribromide (0.38 mL, 4.0 mmol). The mixture was stirred for 10 min, poured into ice water, and extracted twice with methylene chloride. The combined methylene chloride layers were washed once with saturated sodium bicarbonate solution, dried (sodium sulfate), filtered, and concentrated in vacuo. The residue was dissolved in N,N-dimethylformamide (10 mL) and treated with cesium carbonate (652 mg, 2.00 mmol) and methyl bromoacetate (0.28 mL, 2.0 mmol) at room temperature for 3 h. The mixture was diluted with water and extracted three times with ether. The combined ether extracts were washed once with water, dried (magnesium sulfate), filtered, and concentrated in vacuo. Chromatography (silica gel, methylene chloride) provided 479 mg (62%) of the title compound as an off-white solid. 1H NMR (CDCl3) δ 7.25 (m, 3H), 6.85 (d, J=7.6 Hz, 2H), 6.52 (s, 1H), 6.16 (s, 1H), 5.57 (s, 2H), 4.79 (s, 2H), 3.86 (s, 3H), 2.97 (m, 2H), 2.84 (m, 2H), 2.59 (q, J=7.3 Hz, 2H), 1.72 (m, 4H), 1.32 (t, J=7.3 Hz, 3H); MS ES+ m/e 378 (p+1); IR (CHCl3, cm1) 2830, 1756, 1732.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06974831B2
Source datasetuspto-grants-2005_12
ORD IDord-c2fd62053eea44aba55a9cdd87fe4a79
Source noteuspto-grants-2005_12