Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetate | HCID 175 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13603422 | HCID 13603422 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20185127 | HCID 20185127 | 28% |
Reaction Steps
To a solution of 6.0 g. (27.6 mmoles) of 1-ethyl-5-hydroxy-6-allyloxindole in 105 ml. of tetrahydrofuran was added 8.79 g. (27.6 mmoles) of mecuric acetate, and the reaction stirred for 1.5 hours. The mixture was diluted with 29 ml. of 3N sodium hydroxide solution followed by the addition of 522 mg. (13.7 mmoles) of sodium borohydride in 29 ml. of 3N sodium hydroxide solution. The mixture was stirred for 1 hour and was then diluted with diethyl ether and water. The organic phase was washed with water and a saturated brine solution, and then dried over magnesium sulfate. Evaporation of the solvent and chromatographing of the residue on 100 g. of silica gel, using diethyl ether-hexane (1:1, v:v) as the eluent, gave 1.68 g. (28% yield) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04695571 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-88c10bc3d6554369a9f1c50b2c9ac350 |
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| Source note | uspto-grants-1987_09 |
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