Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (S)-(-)-methyl-6-benzyloxy-2,5,7,8-tetramethyl-chroman-2-acetate | HCID 10948608 | — |
| Reactant | Sodium bis(2-methoxyethoxy)aluminiumhydride | HCID 21584525 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 11067787 | HCID 11067787 | — |
Reaction Steps
A 70% solution of sodium bis (2-methoxyethoxy)-aluminum hydride in benzene (35 ml.) was stirred with ice bath cooling while a solution of 20.55 g. (0.0558 mole) of (S)-(-)-methyl-6-benzyloxy-2,5,7,8-tetramethyl- chroman-2-acetate in 50 ml. of benzene was added dropwise over 80 minutes keeping the temperature below 20° C. The resulting solution was stirred at room temperature for 2 hours then cautiously poured onto a mixture of ice and 1 N aqueous NaOH. Work-up by means of ether extraction in the manner of Example 1 afforded 19.8 g. of viscous colorless oil. This material was triturated with petroleum ether (30°-60° C.) and the resulting solid was filtered, washed with petroleum ether and dried under high vacuum giving 14.95 g. (78.7%) of (S)-(-)-6-benzylosy-2,5,7,8-tetramethyl-chroman-2-ethanol as a colorless solid, m.p. 55°-56° C.; [α]25D - 16.21° (c 2.03, CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04051153 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-e16e40617daf4a0fb7603bdf9acd0b4b |
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| Source note | uspto-grants-1977_09 |
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