Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | HCID 19832978 | HCID 19832978 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 19832966 | HCID 19832966 | 15.6% |
Reaction Steps
To a suspension of the crude 2,3-diacetoxy-6-naphthalenesulphonic acid (973 mg) in CCl4 (3 ml) was added phosphorus pentachloride (750 mg). The mixture was heated at 80° C. for 20 minutes, cooled, and water added cautiously. The CCl4 was separated from the aqueous layer and the latter was extracted with CH2Cl2. The organic extracts were combined, washed with water and dried over magnesium sulphate. Evaporation of the solvent yielded 2,3-diacetoxy-6-naphthalenesulphonyl chloride (160 mg, yield: 15%). NMR in CDCl3 : 2.37(s,6H); 7.82(s,1H); 7.87(s,1H); 7.99(s,1H); 8.01(s,1H); 8.54(br.s,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05017569 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-ff946e60bd73417399bf8cc9c3f1b304 |
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| Source note | uspto-grants-1991_05 |
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