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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417315Generated: October 31, 2026

Triethylamine → HCID 57193624, compound

https://huagongshe.com/reaction/417315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Methoxy-4-nitrobenzoic acidHCID 78764—
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantSodium BicarbonateHCID 516892—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 57193624HCID 5719362445%

Reaction Steps

Step A To a solution of 3-methoxy-4-nitrobenzoic acid (Alfa) (10 g, 51 mmol) in toluene (75 mL) was added SOCl2 (11.5 g, 97 mmol), and a catalytic amount of DMF. The mixture was heated at refluxing for 3 h, then cooled to room temperature. The mixture was concentrated. The residue was dissolved into tetrahydrofuran (125 mL) and triethylamine (8.4 g, 83 mmol), and the temperature of the mixture was lowered to 0° C. A hexane solution (Alfa, 2 M) of (trimethylsilyl)diazomethane (41 mL, 83 mmol) was added. The reaction mixture was stirred at room temperature for 18 h. The mixture was poured into an aqueous saturated NaHCO3 solution, extracted with ethyl acetate three times. The combined organic extract was washed with brine, dried over MgSO4, and concentrated to give crude 2-diazo-1-(3-methoxy-4-nitro-phenyl)-ethanone as a brown oil (Yield 5 g, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088815B2
Source datasetuspto-grants-2012_01
ORD IDord-b8e47959b2ae43e09eaa3fc6b5105b81
Source noteuspto-grants-2012_01