Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Methyleneisobenzofuran-1(3H)-one | HCID 10057627 | — |
| Reactant | HCID 53983756 | HCID 53983756 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13071254 | HCID 13071254 | 58.7% |
Reaction Steps
To a solution of o-tolualdehyde chlorooxime (26.8 g, 0.158 mole), 3-methylenephthalide (14.6 g, 0.1 mole) and ether (400 ml.) was added dropwise a solution of triethylamine (16 g, 0.158 mole) in 30 ml. of ether at 5°-10° C. in 45 minutes. The mixture was stirred at room temperature for 40 hours and filtered. The solid material collected was dissolved in 1 liter of chloroform and 200 ml. of water. The chloroform solution was then washed two times with water, dried over CaSO4 and concentrated under vacuum to give 16.4 g of white solid, m.p. 146°-149° C. The original ether solution was washed two times with water, dried over CaSO4 and concentrated to 100 ml. Another 1.64 g of the spiro compound precipitated out. The ether solution was then further concentrated to 10.8 g of yellow-brown oil which did not contain a significant amount of the desired product. Recrystallization of 12 g of the crude spiro compound from tetrahydrofuran-ether gave 9.87 g of a pure white solid, m.p. 159°-164° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04401457 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-f75323e008914209a6f0a0c51d21d7dc |
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| Source note | uspto-grants-1983_08 |
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