Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Lithium diisopropylamide mono(tetrahydrofuran) | HCID 10997623 | — |
| Reactant | HCID 23672793 | HCID 23672793 | — |
| Reactant | HCID 23694644 | HCID 23694644 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 15158732 | HCID 15158732 | — |
Reaction Steps
To a solution of the mixture obtained in Step 2 (100 g) in anhydrous ether (430 ml) was added dropwise 1.5 M lithium diisopropylamide mono(tetrahydrofuran) in cyclohexane (430 ml) under nitrogen atmosphere at -70° C. After stirring for 30 minutes, into the solution was bubbled sulfur dioxide for 1 hour with stirring at -60° C. Then the solution was stirred for 3 hours at room temperature and the formed precipitate was separated by filtration to give a mixture of lithium 4-bromobenzo[b]furan-2-sulfinate and lithium 6-bromobenzo[b]furan-2-sulfinate. To the suspension of the products in dichloromethane (2 1) was added N-chlorosuccinimide (96 g) at -50° C. and stirred for 3 hours under ice-cooling. Insoluble matters were filtered off and dichloromethane was removed in vacuo and the residue was purified by silica gel column chromatography to give 14.1 g of the objective compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05004751 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-fdd6d00775104e9994397231ca007a55 |
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| Source note | uspto-grants-1991_04 |
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