Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | trans-2,2-Dimethyl-3-bromo-6-cyanochroman-4-ol | HCID 6932483 | — |
| Reactant | 3-[(Trimethylsilyl)oxy]pyrrolidin-2-one | HCID 13385941 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 131715947 | HCID 131715947 | — |
Reaction Steps
Sodium hydride (80% dispersion in oil, 1.6 g) was added to a solution of (±)-6-cyano-3,4-dihydro-2,2-dimethyl-trans-3-bromo-4-hydroxy-2H-1-benzopyran (14.86 g) in DMSO (100 mL) and the mixture stirred under a dry atmosphere for 45 min when a solution of the 3,4-epoxide resulted. The solution was then cooled to ca 10° C. before 3-trimethylsilyloxy-2-pyrrolidinone (12.86 g) was added along with further DMSO (20 mL) and sodium hydride (2.35 g). The mixture was stirred at room temperature for 22 h after which it was poured into water (600 mL) and extracted with ethyl acetate several times. The combined extracts were washed with water (4×150 mL), brine and dried (Na2SO4). Evaporation gave a crystalline greenish solid (14.4 g) which was triturated with a little ethyl acetate before filtering under suction and washing with a little ethyl acetate followed by 50% ether/ethyl acetate. The crystalline material (7.9 g, 50%) appeared to be a ca 50:50 mixture of the 3'-hydroxy isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04831050 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-adfea2f81bba4277be10532e21a0908a |
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| Source note | uspto-grants-1989_05 |
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