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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243194Generated: November 3, 2026

Methanesulfonyl chloride → HCID 86608971, compound

https://huagongshe.com/reaction/2243194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 68508938HCID 68508938—
SolventPyridineHCID 1049—
ProductHCID 86608971HCID 86608971—

Reaction Conditions

Temperature2.5 °C

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-trifluoromethylphenoxy)-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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674819B2
Source datasetuspto-grants-2010_03
ORD IDord-ae4588048dc0405d8f26a198f695211d
Source noteuspto-grants-2010_03