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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110883Generated: October 26, 2026

Ethyl orthoformate → 1-(3-Chlorophenyl)-3-(ethoxymethylene)-2(1H,3H)-indolone

https://huagongshe.com/reaction/1110883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactant1-(3-Chlorophenyl)-indolin-2-oneHCID 11299530—
ReactantOrthoformateHCID 21585117—
SolventDiethyl EtherHCID 3283—
Product1-(3-Chlorophenyl)-3-(ethoxymethylene)-2(1H,3H)-indoloneHCID 53712643140.1%

Reaction Steps

1-(3-Chlorophenyl)-2(1H,3H)-indolone (2.4 g, 0.01 mole) and triethyl orthoformate (8.3 ml, 0.05 mole) were combined and heated at 150°±10° for 18 hours. An additional 20 ml of the orthoformate were added and heating continued 2 hours. The reaction mixture was cooled to 25°, diluted with ether, washed with H2O and then brine, dried over MgSO4, concentrated in vacuo to oily solids, and triturated with pentane to yield solids (4.2 g). The solids were chromatographed on silica gel (7.5×15 cm) with 4:1 hexane:ethyl acetate as eluant to yield purified title product, 0.5 g; m.p. 132°-134°; m/e 310/299.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977178
Source datasetuspto-grants-1990_12
ORD IDord-6049152f4c9d43498c7c851d07f2075e
Source noteuspto-grants-1990_12