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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639510Generated: November 3, 2026

Methanesulfonyl chloride → HCID 68577068, compound

https://huagongshe.com/reaction/639510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 59254992HCID 59254992—
SolventDichloromethaneHCID 6344—
ProductHCID 68577068HCID 6857706882%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of compound 31 (5 mg, 0.012 mmol) in dry CH2Cl2 (0.2 mL) was added 4 M HCl dioxane solution (0.5 mL) and stirred for 2 h at 0° C. The solvent was evaporated under reduced pressure. The crude amine salt 32 was dissolved in CH2Cl2 (0.5 mL) and slowly added methanesulfonyl chloride (2 μL, 0.030 mmol) and TEA (9 μL, 0.064 mmol) at 0° C. After 1 h stirring, the reaction mixture was concentrated under reduced pressure. The crude product was purified on a silica gel column chromatography (3:1 n-Hexane/EtOAc) to give a colorless oil (3 mg, 82% yield): 1H NMR (300 MHz, CDCl3) 1.08˜1.87 (m, 20H); 2.36 (d, J=12.4 Hz, 1H); 2.77˜2.92 (m, 5H); 3.51˜3.54 (m, 1H); 4.10˜4.15 (m, 1H); 6.86˜6.96 (m, 2H); 7.13 (d, J=8.3 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691874B2
Source datasetuspto-grants-2010_04
ORD IDord-b210b5eeec3942e0bedd00958cdf4bdb
Source noteuspto-grants-2010_04