Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399545Generated: October 26, 2026

Methanesulfonamide → (S)-1-(3-Chlorophenyl)-2-hydroxy-1-propanone

https://huagongshe.com/reaction/1399545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonamideHCID 72879—
Reactant1-Chloro-3-[(1Z)-1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-propen-1-yl]-benzeneHCID 11300561—
Reactant1-((1R)-((2R,4R,5S)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methoxy)-4-((1R)-((2R,4S,5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methoxy)phthalazineHCID 51003674—
Solvent2-Methylpropan-2-ol--water (1/1)HCID 71401949—
Product(S)-1-(3-Chlorophenyl)-2-hydroxy-1-propanoneHCID 10313420—

Reaction Steps

Compound (S)-10a was synthesized by a procedure similar to that described for (R)-10a using (Z)-tert-butyl(1-(3-chlorophenyl)prop-1-enyloxy)dimethylsilane (9a, 8.8 g, 0.031 mol), AD-mix-α (43.5 g), and CH3SO2NH2 (3a, 3 g, 0.032 mol) in tert-butyl alcohol-water (120 mL:120 mL). The reaction mixture was quenched with sodium sulfite (31.1 g). After purification, 4.51 g (78%) of the (S)-10a was isolated. Characterization data is similar with data reported in Fang, Q. K.; Han, Z.; Grover, P.; Kessler, D.; Senanayake, C. H.; Wald, S. A., Tetrahedron: Asymmetry 2000, 11, 3659-3663.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906908B2
Source datasetuspto-grants-2014_12
ORD IDord-4b2d58a84d4b4a7cb683b16cf81e4086
Source noteuspto-grants-2014_12