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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052756Generated: October 31, 2026

Hydrochloric Acid → HCID 86624775, compound

https://huagongshe.com/reaction/2052756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,6-LutidineHCID 7937—
ReactantEthanesulfonylchloride, 2-chloro-HCID 15385—
ReactantHCID 74062449HCID 74062449—
SolventDichloromethaneHCID 6344—
ProductHCID 86624775HCID 86624775—

Reaction Conditions

Temperature0 °C

Reaction Steps

In 30 mL of CH2Cl2 are dissolved 3.0 g (6.66 mmol) of 2,2,2-Trifluoro-1-(4-{3-[4-(2,2,2-trifluoro-1-hydroxyimino-ethyl)-phenoxy]-propoxy}-phenyl)-ethanone oxime, which is prepared according to the method described in GB 2348644, and the solution is cooled in an ice-bath. To the solution are added successively 2,6-lutidine (3.5 mL, 30.0 mmol) and 2-chloroethanesulfonyl chloride (1.55 mL, 14.7 mmol), and the reaction solution is stirred at 0° C. for 1 h and at room temperature for 2.5 h. Then, it is poured into 1N HCl. The crude product is extracted with CH2Cl2, washed with 1N HCl, dried over MgSO4 and concentrated. The residue is purified by recrystallizaffon from methanol to afford the product as a beige solid. The structure is confirmed by the 1H-NMR spectrum (CDCl3). δ [ppm]: 2.32 (m, 2H), 4.23 (t, 4H), 6.32 (d, 2H), 6.61 (d, 2H), 6.72 (dd, 2H), 7.00 (d, 4H), 7.50 (d, 4H). mp. 84-88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326511B2
Source datasetuspto-grants-2008_02
ORD IDord-407fde0e2aef4c45b8e72d854739397f
Source noteuspto-grants-2008_02