HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-(2-Trimethylsilanylethanesulfonyl)-indole-5-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | methyl 1H-indole-5-carboxylate | HCID 2737635 | — |
| Reactant | 2-(Trimethylsilyl)ethane-1-sulfonyl chloride | HCID 9837086 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Trimethylsilanylethanesulfonyl)-indole-5-carboxylic acid methyl ester | HCID 54384862 | 77.6% |
Reaction Steps
To a solution of 1H-indole-5-carboxylic acid methyl ester (3.6 g, 20.6 mmol) in tetrahydrofuran (180 mL) at 0° C., was added sodium hydride (0.65 g, 21.9 mmol). After 10 min., 2-trimethylsilanylethanesulfonyl chloride (4.4 g, 21.9 mmol) was added and the reaction mixture was allowed to warm to room temperature. After 3 h, acetic acid (1.6 mL, 26.8 mmol) was added and the reaction mixture was concentrated. The crude product was chromatographed (Biotage 40M column, 2.5% ethyl acetate-hexanes) to afford 1-(2-trimethylsilanylethanesulfonyl)-indole-5-carboxylic acid methyl ester (5.43 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492394B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-d7e567e00ed04a6bbe77a4a32ab8ccc0 |
| Source note | uspto-grants-2002_12 |