Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 22758695 | HCID 22758695 | — |
| Product | HCID 22758696 | HCID 22758696 | 90% |
Reaction Steps
206 g of the acid obtained in Example 4 (0.927 mole), 1 liter of CHCl2, are introduced into a triple-tube flask and 1.11 mole of SOCl2 (80 ml) are added with care. The mixture is maintained for 24 hours at 30° C. and the solvents are then removed. Retreatment with 200 ml of benzene is carried out three times by removing the solvent in vacuo each time. 200 g of the product having a melting point of 65° C. (cyclohexane) are thus obtained with a yield of 90%. IR spectrum (KBr) CO: 1670 and 1780 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04127666 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-46f292fc188c455a97170a5cebb6d838 |
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| Source note | uspto-grants-1978_11 |
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