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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589089Generated: October 27, 2026

Triethylamine → N-Methoxy-2-phenyl-3,4-dihydroquinoline-1(2H)-carboxamide

https://huagongshe.com/reaction/589089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant2-Phenyl-1,2,3,4-tetrahydroquinolineHCID 10752915—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductN-Methoxy-2-phenyl-3,4-dihydroquinoline-1(2H)-carboxamideHCID 9040929678.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-phenyl-1,2,3,4-tetrahydroquinoline (2.13 g, 10.2 mmol) and triethylamine (4.26 mL, 30.5 mmol) in tetrahydrofuran (30.0 mL) was added to a solution of triphosgene (3.20 g, 10.8 mmol) in tetrahydrofuran (38.0 mL) at 0° C. The reaction mixture was stirred at 0° C. for 1 h, treated with methoxylamine hydrochloride (1.70 g, 20.3 mmol) and triethylamine (4.26 mL, 30.5 mmol), and stirred at room temperature for an additional 19 h. The reaction mixture was diluted with water (200 mL) and extracted with ethyl acetate (2×100 mL). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered, and concentrated to give a crude oil. Purification by flash column chromatography (100% hexanes to 70% ethyl acetate/hexanes, the ethyl acetate containing 5% methanol) gave the desired product (2.25 g, 78%) as a racemic mixture. LCMS calculated for C17H19N2O2 (M+H)+: m/z=283.1. found: 283.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227985B2
Source datasetuspto-grants-2016_01
ORD IDord-f3dff00d972a49b093aa1c7d25093049
Source noteuspto-grants-2016_01