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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822960Generated: November 1, 2026

Triethylamine → Methyl 7-fluoro-4-methoxy-1-benzothiophene-2-carboxylate

https://huagongshe.com/reaction/1822960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl ThioglycolateHCID 16907—
Reactant2,3-Difluoro-6-methoxybenzaldehydeHCID 2774112—
SolventDimethylformamideHCID 6228—
ProductMethyl 7-fluoro-4-methoxy-1-benzothiophene-2-carboxylateHCID 2217120587.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

Methyl thioglycolate (28.8 mL, 320 mmol) was added under nitrogen to a solution of triethylamine (86.6 mL) in dry N,N-dimethylformamide (220 mL) at 80° C. Stirred at 100° C. for 15 mins. A solution of 2,3-difluoro-6-methoxybenzaldehyde (55.1 g, 320 mmol) in N,N-dimethylformamide (80 mL) was added and the mixture heated at 130° C. for 3 h. Allowed to cool then poured onto ice-water (2 L). The resulting yellow solid was filtered, washing with water (2×200 mL). Dried under vacuum over phosphorus pentoxide at room temperature overnight to give the title compound (67.2 g, 87%); δH (300 MHz, CDCl3) 8.20 (1H, d, ArH), 7.06 (1H, t, ArH), 6.68 (1H, m, ArH) and 3.99 (6H, s, OCH3 and CO2CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037932B2
Source datasetuspto-grants-2006_05
ORD IDord-a8c340c7c4ff40b1a127da3aaa232f14
Source noteuspto-grants-2006_05