Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Chloromethyl pivalate | HCID 87885 | — |
| Reactant | HCID 17933207 | HCID 17933207 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18355318 | HCID 18355318 | 106.1% |
Reaction Steps
To a suspension of sodium hydride (174 mg) in tetrahydrofuran (8.0 ml) was added dropwise a solution of benzyl indole-7-carboxylate (700 mg) in tetrahydrofuran (7.0 ml) at 0° C. and the mixture was stirred at 0° C. for 1 hour. Chloromethyl pivalate (461 mg) was added to the mixture and the solution was stirred at ambient temperature for 3 hours. The reaction was quenched with 1N hydrochloric acid and then the aqueous solution was extracted with ethyl acetate. Drying, filtering and removal of solvents afforded benzyl 1-pivaloyloxymethylindole-7-carboxylate (1.08 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06316482B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-31a1f7250e804faf9f2bdbc2c248fbc7 |
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| Source note | uspto-grants-2001_11 |
|---|