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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642688Generated: October 31, 2026

Phosphorus oxychloride → 5-fluoro-3-formyl-1-naphthalen-1-ylmethyl-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/642688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN-MethylformanilideHCID 66737—
ReactantSodium AcetateHCID 517045—
Reactant5-fluoro-1-naphthalen-1-ylmethyl-1H-indole-2-carboxylic acid ethyl esterHCID 68578393—
Solvent1,2-DichloroethaneHCID 11—
Product5-fluoro-3-formyl-1-naphthalen-1-ylmethyl-1H-indole-2-carboxylic acid ethyl esterHCID 86613189—

Reaction Conditions

Temperature22 °C

Reaction Steps

A mixture of POCl3 (0.79 ml) and N-methylformanilide (1.07 ml) was stirred at 22° C. for 10 min. To the solid formed was added a solution of 5-fluoro-1-naphthalen-1-ylmethyl-1H-indole-2-carboxylic acid ethyl ester (2.00 g from Example 15) in 1,2-dichloroethane (25 ml) and the solution was stirred at reflux temperature for 5 h. The solution was poured into a solution of ice-cold water (40 ml) containing sodium acetate (4.6 g) and stirring was continued at 22° for 2 h. The layers were separated, the aqueous layer extracted with dichloromethane, the combined extracts were dried, evaporated and the residue was chromatographed on silica using n-heptane/AcOEt (10:1) to give 5-fluoro-3-formyl-1-naphthalen-1-ylmethyl-1H-indole-2-carboxylic acid ethyl ester as a colorless solid. MS: 376.4 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696240B2
Source datasetuspto-grants-2010_04
ORD IDord-039b3d425b94433d934a50f53a1e0e18
Source noteuspto-grants-2010_04