HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073Generated: October 26, 2026
Sulfuryl chloride → 4-(Benzyloxy)benzene-1-sulfonyl chloride
https://huagongshe.com/reaction/1073
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Benzyl Phenyl Ether | HCID 70352 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Benzyloxy)benzene-1-sulfonyl chloride | HCID 4738385 | — |
Reaction Steps
A 1.12 portion of anhydrous DMF is cooled to 0° C. and treated dropwise with 2.06 g of sulfuryl chloride. The resulting suspension is stirred for 30 min., then treated with 1.50 g of benzyl phenyl ether. The mixture is heated at 90° C. for 3 h, then cooled, extracted with brine and methylene chloride, and dried over MgSO4. Chormotography on silica gel (i-PrOH/hexanes) yields 4-benzyloxybenzenesulfonyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05723490 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-7b357d5bf4334f0fb405475a558ece52 |
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| Source note | uspto-grants-1998_03 |
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