CAS: 675-20-7
MF: C5H9NO
Appearance: white to yellowish low melting crystalline mass
Preparation |
2-Piperidone can be obtained from cyclopentanone as raw material by a two-step reaction. |
Synthesis Reference(s) |
Journal of the American Chemical Society, 102, p. 7629, 1980 DOI: 10.1021/ja00546a001Tetrahedron Letters, 28, p. 2829, 1987 DOI: 10.1016/S0040-4039(00)96220-8The Journal of Organic Chemistry, 21, p. 965, 1956 DOI: 10.1021/jo01115a010 |
Purification Methods |
Purify it by repeated fractional distillation.[Cowley J Org Chem 23 1330 1958, Reppe et al. Justus Liebigs Ann Chem 596 198 1955, IR: Huisgen et al. Chem Ber 90 1437 1957.] The hydrochloride has m 183-184o (from isoPrOH or EtOH/Et2O) [Hurd et al. J Org Chem 17 865 1952], and the oxime has m 122.5o (from pet ether) [Behringer & Meier Justus Liebigs Ann Chem 607 67 1957]. The picrate has m 92-93o. [Beilstein 21 H 239, 21 III/IV 3170, 21/6 V 396.] |
Definition |
ChEBI: 2-Piperidone is a delta-lactam that is piperidine which is substituted by an oxo group at position 2. It has a role as an EC 1.2.1.88 (L-glutamate gamma-semialdehyde dehydrogenase) inhibitor. It is a member of piperidones and a delta-lactam. |
InChI:InChI=1/C5H9NO/c7-5-3-1-2-4-6-5/h1-4H2,(H,6,7)
The invention provides a method for sele...
PROBLEM TO BE SOLVED: To provide an indu...
We report a highly atom-efficient integr...
Peptide bond formation is a challenging,...
piperidine
2,3,4,5-tetrahydropyridine
piperidin-2-one
Conditions | Yield |
---|---|
piperidine;
With
chloroamine; sodium hydroxide;
In
water;
at 25 ℃;
pH=12.89;
With
water;
|
methanol
cyclopentanone oxime tosylate
2,3,4,5-tetrahydro-6-methoxypyridine
piperidin-2-one
Conditions | Yield |
---|---|
|
2-hydroxypyridin
piperidine-2-thione
3,4,5,6-tetrahydro-2H-pyran-2-one
methanol
5-(N-phthalimido)pentanoic acid
N-acetyl-2-piperidone
7,8,9-trihydropyrido[2,1-b]quinazolin-11(6H)-one
piperidine-2-thione