Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 23118300 | HCID 23118300 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23118277 | HCID 23118277 | 100.3% |
Reaction Steps
To 10 g of 6-nitro-2-methoxymethyl-2,5,7,8-tetramethylchroman-4-one, 100 ml of methanol was added and 1.3 g of sodium borohydride was added at 0° C., followed by stirring at 0° C. for one hour. The reaction solution was poured into water and then extracted with ethyl acetate. The organic layer was washed with saturated saline and then dried over anhydrous magnesium sulfate. After removing magnesium sulfate by filtration and concentrating under reduced pressure, 10.1 g of the objective compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07553837B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-4c243370f2b84c3eafab865e038e3359 |
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| Source note | uspto-grants-2009_06 |
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