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15519

Sigma-Aldrich

1-Boc-4-piperidone

puriss., ≥99.0% (HPLC)

Synonym(s):

N-Boc-4-piperidone, tert-Butyl 4-oxo-1-piperidinecarboxylate

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About This Item

Empirical Formula (Hill Notation):
C10H17NO3
CAS Number:
79099-07-3
Molecular Weight:
199.25
Beilstein/REAXYS Number:
3650236
MDL number:
MFCD00151800
UNSPSC Code:
12352100
PubChem Substance ID:
329750922

grade

puriss.

assay

≥99.0% (HPLC)

mp

73-77 °C (lit.)
73-77 °C

SMILES string

CC(C)(C)OC(=O)N1CCC(=O)CC1

InChI

1S/C10H17NO3/c1-10(2,3)14-9(13)11-6-4-8(12)5-7-11/h4-7H2,1-3H3

InChI key

ROUYFJUVMYHXFJ-UHFFFAOYSA-N

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Application

1-Boc-4-piperidone was used in the preparation of anti-aldol product with fair diastereo- and enantioselectivity[1].

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Dorota Gryko et al.
Organic & biomolecular chemistry, 5(13), 2148-2153 (2007-06-22)
Water was found to be a suitable solvent for the l-prolinethioamide catalysed aldol reaction of various cyclic ketones with aromatic aldehydes. Treatment of 4-nitrobenzaldehyde with as little as 1.2 equiv. of cyclohexanone in the presence of the protonated catalyst 1-TFA

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