Methanesulfonyl chloride → HCID 86588786, compound

HRID 2220087Notes

Reaction equation

HRID 2220087 reaction equation
[CH2:1]([N:5]1[CH2:10][CH2:9][CH:8]([C:11]2[CH:12]=[C:13]([OH:17])[CH:14]=[CH:15][CH:16]=2)[CH2:7][CH2:6]1)[CH2:2][CH2:3][CH3:4].[CH3:18][S:19](Cl)(=[O:21])=[O:20]>>[CH2:1]([N:5]1[CH2:10][CH2:9][CH:8]([C:11]2[CH:12]=[C:13]([O:17][S:19]([CH3:18])(=[O:21])=[O:20])[CH:14]=[CH:15][CH:16]=2)[CH2:7][CH2:6]1)[CH2:2][CH2:3][CH3:4]

Participants

3

Reactant 2

HCID 31297Methanesulfonyl chlorideHCID 22397835HCID 22397835, compound

Product 1

HCID 86588786HCID 86588786, compound

Procedure

Beginning with 3-(1-butyl-piperidin-4-yl)-phenol and methanesulfonyl chloride. MS m/z (rel. intensity, 70 eV) 311 (M+, 3), 268 (bp), 189 (20), 131 (18), 79 (12);

Sources & evidence

ORD record
ord-3655ebb79bfd49cd811996db6980ad27
Source dataset
uspto-grants-2008_08
Patent number
US07417043B2

Reaction notes

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