Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanic acid | HCID 540 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Dibenzyl ether | HCID 7657 | — |
Reaction Steps
To a slurry of 1.1 g of sodium hydride (21 mmole, 50% oil dispersion) in 25 ml of dry DMF at 0° C. was added a solution of 3.34 g of Example 1 Part G cyanoalcohol (20 mmole) in 10 ml of DMF over a period of 10 minutes. After stirring for an additional b 15 minutes, 3.6 g of benzyl bromide was added dropwise. The reaction mixture was stirred for 30 minutes at 0° C. and 3 hours at 25° C. then quenched with a saturated ammonium chloride solution, and diluted with ether. The organic layer was washed with brine. The combined aqueous layer was re-extracted with ether. The combined organic layer was dried over anhydrous MgSO4 and concentrated to leave an oil. The crude oil was chromatographed on a silica gel column, eluting with 10-20% ethyl acetate in hexanes to give 4.43 g of the title A benzyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04654366 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-206b7d427acc4bba9e6274272b6f6d73 |
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| Source note | uspto-grants-1987_03 |
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