Cyclobutanecarbonyl chloride → HCID 15289311, compound

HRID 1457769Notes

Reaction equation

HRID 1457769 reaction equation
[CH2:1]([CH:10]1[CH2:15][CH2:14][CH2:13][CH2:12][NH:11]1)/[CH:2]=[CH:3]/[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH:16]1([C:20](Cl)=[O:21])[CH2:19][CH2:18][CH2:17]1>>[CH2:1]([CH:10]1[CH2:15][CH2:14][CH2:13][CH2:12][N:11]1[C:20]([CH:16]1[CH2:19][CH2:18][CH2:17]1)=[O:21])/[CH:2]=[CH:3]/[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH2:1]([CH:10]1[CH2:15][CH2:14][CH2:13][N:11]1[C:20]([CH:16]1[CH2:19][CH2:18]1)=[O:21])/[CH:2]=[CH:3]/[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1

Participants

4

Reactant 2

HCID 78705Cyclobutanecarbonyl chlorideHCID 10878208HCID 10878208, compound

Product 2

HCID 15289311HCID 15289311, compoundHCID 19367175HCID 19367175, compound

Procedure

Stage a) The method is the same as that of Example 1.1, Stage a), the initial reactants being (E)-2-(cinnamyl)piperidine and cyclobutanecarboxylic acid chloride, which furnish (E)-2-cinnamyl-1-(cyclobutanecarbonyl)piperidine (formula II; Ar=C6 H5, m=1, n=2, R=cyclobutyl). Yield: 99%.

Sources & evidence

ORD record
ord-4d1f690645f7455a9bb10ad3aa2008e8
Source dataset
uspto-grants-1998_12
Patent number
US05849760

Reaction notes

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