HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487663Generated: October 29, 2026
Tetrahydrofuran → HCID 19092856, compound
https://huagongshe.com/reaction/487663
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 19092862 | HCID 19092862 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19092856 | HCID 19092856 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05296499 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-d6691a02d6bb4bde938660d0c6ea2810 |
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| Source note | uspto-grants-1994_03 |
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