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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487663Generated: October 29, 2026

Tetrahydrofuran → HCID 19092856, compound

https://huagongshe.com/reaction/487663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 19092862HCID 19092862—
CatalystDimethylformamideHCID 6228—
ProductHCID 19092856HCID 1909285670%

Reaction Steps

N,N-Dimethylformamide (3 drops) and oxalyl chloride (0.59 ml) were added to a solution of 5,6-dimethoxy-3-(3,4-dimethoxyphenyl)indole-2-carboxylic acid (2.0 g) in tetrahydrofuran (50 ml). The mixture was stirred for an hour at room temperature and concentrated under reduced pressure. The residue was dissolved in benzene (20 ml). This benzene solution was added to a solution of tert-butanol (0.79 ml) and N,N-dimethylaniline (0.85 ml) in benzene (30 ml), followed by stirring overnight at room temperature. The mixture was successively washed with water, sodium hydrogen carbonate saturated aqueous solution and water, dried (MgSO4) and concentrated. The precipitated crystals were collected by filtration and recrystallized from acetone to give tert-butyl 5,6-dimethoxy-3-(3,4-dimethoxyphenyl)indole-2-carboxylate (1.61 g, 70%) as colorless prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05296499
Source datasetuspto-grants-1994_03
ORD IDord-d6691a02d6bb4bde938660d0c6ea2810
Source noteuspto-grants-1994_03