Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 7-bromoisochroman | HCID 10560525 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20086443 | HCID 20086443 | — |
Reaction Steps
A solution of 7-bromoisochroman (6.6 g; 30.98 mmol) in THF (100 ml) was cooled to -78° C. and treated with 2.1 eq of tert-butyllithium (40 ml of a 1.7M solution). After stirring the solution for one minute, iodine (8.64 g; 34.08 mmol) was added as a THF solution (50 ml). The reaction mixture was stirred for 30 minutes at -78° C. and one hour at room temperature. It was quenched with saturated aqueous ammonium chloride, and the organic phase was washed with aqueous sodium thiosulfate and brine, dried, and freed of solvent. The crude product was recrystallized from hexane to provide the pure 5-iodoisochroman as a white crystalline solid, mp= 54°-56° C. (4.1 g; 51%). 1H NMR (CDCl3): δ2.79 (t, 2H); 3.94 (t, 2H); 4.70 (s, 2H); 6.85 (d, 1H); 7.32 (s, 1H); 7.46 (d, 1H). IR (nujol): 2931, 2852, 1550, 1252, 1190, 1105, 1005, 987 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05395827 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-0b5988a505e44fe88e95811fd5087d2f |
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| Source note | uspto-grants-1995_03 |
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