Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 136092599 | HCID 136092599 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 136032768 | HCID 136032768 | — |
Reaction Steps
Thionyl chloride (120 ml) was added with stirring to a suspension of VI (11.1 g, 0.026 mole) in dry tetrahydrofuran (120 ml) at 20° C. The mixture became warm and the suspension dissolved, giving a dark-red solution. After a few minutes, a bright-red solid precipitated. The mixture was stirred for a further 15 minutes, cooled to 5° C. and the product filtered off and dried at 50° C. for one hour. TLC analysis showed the product to be pure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04250238 |
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| Source dataset | uspto-grants-1981_02 |
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| ORD ID | ord-935168a2e844495c97b34c1632c44e16 |
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| Source note | uspto-grants-1981_02 |
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