HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472133Generated: October 29, 2026
Oxalyl chloride → 4-(2-Methylquinolin-4-ylmethoxy)benzenesulfonyl chloride hydrochloride
https://huagongshe.com/reaction/472133
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 4-(2-Methylquinolin-4-ylmethoxy)benzenesulfonic acid | HCID 21963051 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(2-Methylquinolin-4-ylmethoxy)benzenesulfonyl chloride hydrochloride | HCID 86607865 | 92% |
Reaction Steps
76 g (216 mmol) of the sodium salt of 4-(2-methylquinolin-4-ylmethoxy)benzenesulfonic acid in 500 ml of dimethylformamide are added dropwise to a solution of 55 ml (649 mmol) of oxalyl chloride in 100 ml of dichloromethane, cooled beforehand to −10° C. After the addition, the reaction medium is stirred at ambient temperature for 18 h. The reaction medium is then poured into 11 of ice and then extracted with ethyl acetate. The organic phases are combined, washed with water and then with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, filtered and concentrated under vacuum. 77 g (92%) of 4-(2-methylquinolin-4-ylmethoxy)benzenesulfonyl chloride hydrochloride are obtained in the form of a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633196B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-3d6d395d09a94c4fb946ac3ffac1571b |
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| Source note | uspto-grants-2014_01 |
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