Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,1-Diphenylethylene | HCID 10740 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Product | HCID 12218100 | HCID 12218100 | 29% |
Reaction Steps
1,1-Diphenylethene (11.3 mmol, 2 ml) was added to a solution of DMF (22.7 mmol, 1.75 ml) and sulfuryl chloride (19.3 mmol, 1.55 ml) at 0° C. The reaction was heated to 90° C. for 4 hr, then cooled to ambient temperature and poured into ice (500 ml). The aqueous layer was extracted with EtOAc (2×100 ml). Then the organic was dried (MgSO4) filtered and concentrated. Flash chromatography (5% EtOAc/hexane) provided 0.92 g (29% yield) of light yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05571821 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-b0900369af114a5796d1a1ca84a02359 |
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| Source note | uspto-grants-1996_11 |
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