Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 67290361 | HCID 67290361 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86664425 | HCID 86664425 | — |
Reaction Steps
Sulphur dioxide was bubbled into a flask with acetic acid (10 mL) and cupric chloride (62 mg 0.63 mmol) until the green solution turned into blue. 3-(6-chloro-4,4-dimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenylamine (600 mg 2.09 mmol) was dissolved in a aceticacid (27 mL) and hydrochloric acid (3 mL) solution, and cooled to −10° C., sodium nitrite (213 mg, 3.09 mmol) in water (2 mL) solution was added and the mixture was stirred for 45 min. sulphur dioxide solution was added dropwise to the diazonium salt solution and stirred at −10° C. After the addition, the solution was warmed to room temperature and stirred for 24 h. The mixture was poured to 100 mL water and extracted with dichloromethane. The combined organic layers was washed with sodium bicarbonate and dried. Removal of the solvent afforded 3-(6-chloro-4,4-dimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-benzenesulfonyl chloride as yellow solid (crude 98 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546427B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-c345ced3c4f34820b81b1a861fa5833e |
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| Source note | uspto-grants-2013_10 |
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