Methanesulfonyl chloride → HCID 86588785, compound

HRID 2220086Notes

Reaction equation

HRID 2220086 reaction equation
[CH2:1]([N:3]1[CH2:8][CH2:7][CH:6]([C:9]2[CH:10]=[C:11]([OH:15])[CH:12]=[CH:13][CH:14]=2)[CH2:5][CH2:4]1)[CH3:2].[CH3:16][S:17](Cl)(=[O:19])=[O:18]>>[CH2:1]([N:3]1[CH2:8][CH2:7][CH:6]([C:9]2[CH:10]=[C:11]([O:15][S:17]([CH3:16])(=[O:19])=[O:18])[CH:12]=[CH:13][CH:14]=2)[CH2:5][CH2:4]1)[CH3:2]

Participants

3

Reactant 2

HCID 31297Methanesulfonyl chlorideHCID 22397828HCID 22397828, compound

Product 1

HCID 86588785HCID 86588785, compound

Procedure

Beginning with 3-(1-ethyl-piperidin-4-yl)-phenol and methanesulfonyl chloride. MS m/z (rel. intensity, 70 eV) 283 (M+, 6), 268 (bp), 189 (54), 131 (20), 79 (70);

Sources & evidence

ORD record
ord-065ad59cef314f378de62280692a3dec
Source dataset
uspto-grants-2008_08
Patent number
US07417043B2

Reaction notes

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