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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071133Generated: November 2, 2026

Ethylene Glycol → 10-(2-Fluorophenyl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole

https://huagongshe.com/reaction/1071133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantPotassium HydroxideHCID 14797—
ReactantAmmonium HydroxideHCID 14923—
Reactant3-Benzoyl-10-(2-fluorophenyl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indoleHCID 22396693—
SolventWaterHCID 962—
SolventChloroform methanolHCID 21584188—
Product10-(2-Fluorophenyl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indoleHCID 22396700—

Reaction Steps

3-Benzoyl-10-(2-fluorophenyl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole (3.50 g, 9.1 mmol), potassium hydroxide (11.80 g, 183 mmol), and ethylene glycol (80 mL) were heated to 170° C. for 6.6 hours. The reaction was diluted with water and extracted with ethyl acetate. The organic layers were combined, washed with brine, dried over MgSO4 and concentrated in vacuo to give a red oil which was passed through a column of silica gel with 1:19 methanol/chloroform with 1% NH4OH to give 2.43 g (95%) of a white solid as the title compound: mp 121.8-126.3° C. 1H NMR (400 MHz, CDCl3) δ 8.02 (br s, 1H), 7.42-7.34 (m, 3H), 7.26-7.16 (m, 3H), 6.98 (d, J=7.2 Hz, 1H), 3.16-2.86 (m, 6H), 2.58-2.53 (m, 1H), 2.46-2.39 (m, 1H); MS m/z 281.2 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903090B2
Source datasetuspto-grants-2005_06
ORD IDord-ba9de0adff5745ab98a42885abfc37db
Source noteuspto-grants-2005_06