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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051389Generated: November 1, 2026

Methanesulfonyl chloride → HCID 90133853, compound

https://huagongshe.com/reaction/1051389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 118323818HCID 118323818—
SolventDichloromethaneHCID 6344—
ProductHCID 90133853HCID 9013385395%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 50 mL round-bottomed flask, 3,3,3-trifluoro-2-((2-(3-(trifluoromethyl)phenyl)morpholino)-methyl)propan-1-ol (760 mg, 2.13 mmol) was combined with CH2Cl2 (10.0 ml) to give a colorless solution and then cooled to 0° C. DIPEA (412 mg, 557 μl, 3.19 mmol) and methanesulfonyl chloride (244 mg, 166 μl, 2.13 mmol) were added dropwise and the resulting reaction mixture was stirred for 30 min. The reaction was diluted with CH2Cl2 (30 ml), washed with sat. NaHCO3 solution followed by washing with H2O, dried over MgSO4, filtered and concentrated to give 880 mg (95%) of methanesulfonic acid 3,3,3-trifluoro-2-[2-(3-trifluoromethyl-phenyl)-morpholin-4-ylmethyl]-propyl ester as a colorless oil. MH+=436.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388172B2
Source datasetuspto-grants-2016_07
ORD IDord-6a43035d99234a92b612b82f907101c3
Source noteuspto-grants-2016_07