HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216276Generated: October 30, 2026
Acetic Acid → [4-(Chlorosulfonyl)phenyl]methylene diacetate
https://huagongshe.com/reaction/216276
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Product | [4-(Chlorosulfonyl)phenyl]methylene diacetate | HCID 11849277 | 38% |
Reaction Steps
A solution of p-toluenesulfonyl chloride (40.2 g) in acetic acid:acetic anhydride (800 mL, 1:1) was treated with conc. sulfuric acid (64 mL, 5 equivalents) at 0-5° C. Chromium trioxide (80 g, 4 equivalents) was added at such a rate that the temperature remained below 10° C. The mixture was stirred at 5-10° C. until reaction was completed as indicated by TLC. The mixture was quenched with ice water (2 L), and the solids were filtered, washed with water, and dried. The solids were combined with saturated NaHCO3 (1 L) at 25° C. for 2 hrs, filtered, dissolved in dichloromethane (1 L), dried over Na2SO4, filtered and concentrated. The residue was recrystallized from 2-3 volumes of hot acetone/pentane and cooling for 16 hrs. The crystals are filtered, and washed with cold pentane to give the product (24 g, 38%). 1H NMR (CDCl3): δ 8.09 (d, J=9 Hz, 2H), 7.77 (d, J=9 Hz, 2H), 7.73 (s, 1H), 2.16 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193227B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-8f66a9e2b0d44de4b6d149af4c89e7bb |
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| Source note | uspto-grants-2012_06 |
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