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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215819Generated: October 29, 2026

Methanol → HCID 21950033, compound

https://huagongshe.com/reaction/2215819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantOxalyl chlorideHCID 65578—
Reactant5-(trifluoromethyl)-1H-indoleHCID 2763075—
ReactantSodium MethoxideHCID 10942334—
SolventDiethyl EtherHCID 3283—
ProductHCID 21950033HCID 2195003343%

Reaction Steps

To a solution of 5-trifluoromethylindole (2.0 g, 10.8 mmol) in diethyl ether (30 mL) at 4° C. was added a 2.0 M solution of oxalyl chloride in methylene chloride (5.5 mL, 11.0 mmol). The resulting solution was allowed to warm to room temperature. After 90 min, the solution was cooled to −78° C. To this solution was added 25% (w/w) solution of sodium methoxide in methanol (5.0 mL, 21.9 mmol). The resulting solution was allowed to warm to room temperature. After one hour, the solution was filtered to give the title compound (1.24 g, 43%) as a yellow solid. 1H NMR (DMSO-d6) δ 8.66 (m, 1H), 8.45 (s, 1H), 7.78 (m, 1H), 7.60 (m, 1H), 3.89 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109229B2
Source datasetuspto-grants-2006_09
ORD IDord-5bc08e1385094d95a62c4d449881e7f9
Source noteuspto-grants-2006_09