Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-(4-Chloro-2-fluorophenyl)-4,5,6,7-tetrahydro-1h-isoindole-1,3(2h)-dione | HCID 185931 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21496693 | HCID 21496693 | — |
Reaction Steps
Twenty parts of a 3.13M methylmagnesium chloride solution in tetrahydrofuran was added dropwise to a solution of 20 parts of 2-(4-chloro-2-fluorophenyl)-4,5,6,7-tetrahydro-2 H-isoindole-1,3-dione in 200 parts of anhydrous tetrahydrofuran at 0° C over 1/2 hour. After stirring for 2 hours at 0° , 10 parts of a saturated aqueous ammonium chloride was added dropwise at 0°, resulting in a granular precipitate. After filtering the precipitate, the filtrate was evaporated at 300 mm. Hg and 50° to give 23.5 parts of 2-(4-chloro-2-fluorophenyl) -2,3,4,5,6,7-hexahydro-3-hydroxy-3methyl-1H-isoindol-1-one as indicated in particular by adsorption in the infrared spectrum of 1690 cm-1 (amide) and 3300 cm-1 (hydroxyl) and in the nuclear magnetic resonance spectrum of 4.6δ (1H, hydroxyl) and 1.1δ (3H, singlet methyl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03992189 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-0aee8768703c4f41bacb002c15ab6d19 |
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| Source note | uspto-grants-1976_11 |
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