HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224060Generated: October 31, 2026
Chloroacetyl chloride → HCID 22312860, compound
https://huagongshe.com/reaction/2224060
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Amino-4-phenylsulfonylphenol | HCID 13366036 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22312860 | HCID 22312860 | 92% |
Reaction Steps
2-Amino-4-benzenesulfonyl-phenol (2.064 g, 8.2 mmol) was dissolved in 15 mL of methyl ethyl ketone, and NaHCO3 (1.39 g, 9.1 mmol) was added to this solution. The reaction mixture was cooled to 0° C., and 2-chloroacetyl chloride (0.215 mL, 9.0 mmol) was added dropwise while stirring. The reaction mixture was stirred for 2 hours, after which K2CO3 (1.37 g, 9.95 mmol) was added, and the reaction was brought to reflux for three hours. The reaction mixture was cooled and 150 mL of EtOAc was added. The organic layer was washed three times with 50 ml water, once with 50 mL saturated brine, dried (Na2SO4) and concentrated in vacuo to yield a crude solid, which was purified by flash chromatography (10-30% EtOAc in hexanes), to afford 6-benzenesulfonyl-4H-benzo[1,4]oxazin-3-one (2.176 g, 7.52 mmol, 92%). MS: 290 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07378415B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-7164fdef660641b1b6783a38f50cf315 |
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| Source note | uspto-grants-2008_05 |
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