2-Piperidone → HCID 18916099, compound

HRID 1290574Notes

Reaction equation

[CH3:1][CH2:2][CH2:3][CH:4]([S:8]([C:11]1[CH:26]=[CH:25][CH:24]=[CH:23][C:12]=1[C:13]([N:15]1[CH2:21][CH2:20][CH2:19]C[CH2:17][C:16]1=[O:22])=[O:14])(=[O:10])=[O:9])[CH2:5][CH2:6][CH3:7].C1(=O)NCCCC1>>[CH3:1][CH2:2][CH2:3][CH:4]([S:8]([C:11]1[CH:26]=[CH:25][CH:24]=[CH:23][C:12]=1[C:13]([N:15]1[CH2:21][CH2:20][CH2:19][CH2:17][C:16]1=[O:22])=[O:14])(=[O:9])=[O:10])[CH2:5][CH2:6][CH3:7]

Participants

Reactant 2

HCID 126652-Piperidone

HCID 18916094HCID 18916094, compound

Product 1

HCID 18916099HCID 18916099, compound

Procedure

Synthesized as for N-[(4-heptylsulfonyl)benzoyl]caprolactam (Example VII) using valerolactam (Aldrich) in place of caprolactam.

Sources & evidence

ORD record: ord-3a213ec16f9c4cc3939aab344d45238d
Source dataset: uspto-grants-1998_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05753138

Reaction notes

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