HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874574Generated: October 29, 2026
Oxalyl chloride → 4-(2-Methylquinolin-4-ylmethoxy)benzenesulfonyl chloride hydrochloride
https://huagongshe.com/reaction/874574
Participants
| Role | Name | HCID | Charge |
|---|
| 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 1 l 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 | US08980897B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-d6f8cb0e19f6467ea0384c06c4929207 |
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| Source note | uspto-grants-2015_03 |
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