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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193486Generated: October 31, 2026

Ethanol → HCID 21272043, compound

https://huagongshe.com/reaction/1193486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 54540393HCID 54540393—
SolventDiethyl EtherHCID 3283—
ProductHCID 21272043HCID 2127204394%

Reaction Steps

Oxalyl chloride (3.2 g, 2.2 mL, 24.7 mmol) was added dropwise under nitrogen to an ice cold solution of ethyl 7-(phenylmethoxy)-indole (2.3 g, 10.3 mmol) in anhydrous ether (40 mL). The mixture was stirred for 1 hour at room temperature during which time a yellow precipitate was formed. The solvent and the excess of oxalyl chloride was removed at reduced pressure to yield 7-(phenylmethoxy)-indol-3-yl-glyoxyl chloride. Ethanol (50 mL) was then added to the residue and the solution was stirred overnight under nitrogen at room temperature. Removal of the solvent in vacuo provided ethyl 7-(phenylmethoxy)-indol-3-yl-glyoxylate as a tan solid (3 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04810699
Source datasetuspto-grants-1989_03
ORD IDord-80bc4b64268849269feb2c47b02fcd26
Source noteuspto-grants-1989_03