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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982028Generated: October 27, 2026

Phosphorus oxychloride → Benzyl 3-Formylindole-2-carboxylate

https://huagongshe.com/reaction/982028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN-MethylformanilideHCID 66737—
Reactantbenzyl 1H-indole-2-carboxylateHCID 7723355—
ReactantAcetic acid, sodium salt, monohydrateHCID 23681166—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductBenzyl 3-Formylindole-2-carboxylateHCID 1458346480.3%

Reaction Steps

A mixture of 6.5 ml (70 mmol) of phosphorus oxychloride and 9.3 ml (70 mmol) of N-methylformanilide was stirred at ambient temperature. The resulting mixture was diluted with 90 ml of 1,2-dichloroethane, treated with 15.0 g (59.8 mmol) of benzyl indole-2-carboxylate, and heated at reflux for 1 h. After being allowed to cool for 5 min, the warm solution was poured into an ice-cold solution of 60 g of sodium acetate hydrate in 200 ml of water. The resulting mixture was stirred for 1 h, filtered, and the yellow solid was washed twice with water and twice with ether, and air-dried. The filtrate was treated with 400 ml of hexane and filtered. The combined solids were digested with hot ethyl acetate, cooled to 0° C., and filtered to give 13.41 g (80%) of the desired compound as an off-white solid. 1H NMR (CDCl3 /CD3OD) δ 5.50 (s,2H), 7.3-7.55 (m, 8H), 8.38 (d,J=9 Hz,1H). Mass spectrum: (M+H)+ =280.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994477
Source datasetuspto-grants-1991_02
ORD IDord-1a1dea1bf6a14f3e8b7127447387af93
Source noteuspto-grants-1991_02