Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | 5-Bromo-2,2-diphenyl-1,3-benzodioxol | HCID 22319515 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 67783234 | HCID 67783234 | — |
Reaction Steps
A solution of butyllithium (0.6M) (74 ml) in n-hexane are mixed with 116 ml of diethyl ether and cooled to -55° C. Thereupon, a solution of 40.0 g of 5-bromo-2,2-diphenyl-1,3-benzodioxol in 170 ml of diethyl ether is added dropwise. The reaction mixture is stirred for 1 hour, whereby the temperature rises to -15° C. Subsequently, the mixture is cooled to -50° C. and dry sulphur dioxide gas is introduced for 45 minutes. The excess sulphur dioxide gas is removed by passing dry argon through the mixture for 1 hour. The reaction mixture is left to come to room temperature. There thereby results a white precipitate, which is filtered off and dried. There are obtained 22.2 g of 2,2-diphenyl-1,3-benzodioxol-5-sulphinic acid lithium salt as white crystals of m.p.>300° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05438052 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-99ac9ad8b954402ca2d826cabfd2fdc3 |
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| Source note | uspto-grants-1995_08 |
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