HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715321Generated: October 29, 2026
Methanesulfonyl chloride → HCID 86608971, compound
https://huagongshe.com/reaction/1715321
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 68508938 | HCID 68508938 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86608971 | HCID 86608971 | — |
Reaction Steps
Methanesulfonyl chloride (36.45 g, 318 mmol) was added in one portion to a cold (0-5° C.) sol'n of the N-sec-butyl-2-(4-cyano-3-trifluoromethyl phenoxy)-4-hydroxy-3,3-dimethylbutyramide (5, 79.0 g, 212 mmol) in 200 mL pyridine. The reaction mixture was stirred at 0-5° C. for 5 h. The reaction was quenched with 800 mL sat'd aq. NH4Cl and extracted with 1000 mL CH2Cl2. The organic phase was washed with 2N aq. HCl (3×300 mL) and then half sat'd aq. NaCl (3×300 mL). The organic was conc'd under vac (35-40° C.) to an amber gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07799823B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-f86a7dde619f44178e98fbcf842f9bf0 |
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| Source note | uspto-grants-2010_09 |
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