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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360128Generated: October 29, 2026

Methanesulfonyl chloride → HCID 57425777, compound

https://huagongshe.com/reaction/1360128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57425775HCID 57425775—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
ProductHCID 57425777HCID 57425777—

Reaction Steps

To the solution of 1-(4-fluorophenyl)-2,2-dipyridin-3-ylethanol (0.2 g, 0.68 mmol) in THF (4 mL) was added i-Pr2NEt (0.4 mL, 2.3 mmol) at 0° C. followed by methanesulfonyl chloride (0.1 mL, 1.3 mmol). The reaction mixture was stirred for 10 h. Diluted with saturated NaHCO3 and extracted with CH2Cl2. The combined organic layer was dried, filtered, and concentrated to give 1-(4-fluorophenyl)-2,2-dipyridin-3-ylethyl methanesulfonate. LRMS m/z (M+H) Calcd: 373.4. found: 373.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879839B2
Source datasetuspto-grants-2011_02
ORD IDord-b45371c9c54c466aa8b94c9e5b2dd0bf
Source noteuspto-grants-2011_02