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Chemical Structure| 2403-88-5 Chemical Structure| 2403-88-5
Chemical Structure| 2403-88-5

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Product Details of 2,2,6,6-Tetramethyl-4-piperidinol

CAS No. :2403-88-5
Formula : C9H19NO
M.W : 157.25
SMILES Code : CC1(C)CC(O)CC(C)(C)N1
MDL No. :MFCD00005983
InChI Key :VDVUCLWJZJHFAV-UHFFFAOYSA-N
Pubchem ID :75471

Safety of 2,2,6,6-Tetramethyl-4-piperidinol

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314-H317
Precautionary Statements:P280-P305+P351+P338-P310
Class:8
UN#:3259
Packing Group:

Application In Synthesis of 2,2,6,6-Tetramethyl-4-piperidinol

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 2403-88-5 ]

[ 2403-88-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 2403-88-5 ]
  • [ 1202-25-1 ]
  • 1-(2,2,6,6-tetramethylpiperidine-4-yl)-4-(N,N-dimethylamino)benzoate [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 1 A mixture of 18 g of methyl p-dimethylaminobenzoate, 15.7 g of 2,2,6,6-tetramethyl-4-hydroxypiperidine and 0.2 ml tetrabutyl ortotitanate is heated and stirred for 6 hours at 170 C. The reaction product is recrystallized from petroleum ether at 100/120 C. and decolourized with decolourizing earth. 4-(p-dimethylamino-benzoyloxy)-2,2,6,6-tetramethylpiperidine is obtained in form of a crystalline white substance with m.p. 137-139 C. and specific extinction (E:)--992 at 312 nm.
EXAMPLE 1 A mixture of 18 g of methyl p-dimethylaminobenzoate, 15.7 g of 2,2,6,6-tetramethyl-4-hydroxypiperidine and 0.2 ml tetrabutyl ortotitanate is heated and stirred for 6 hours at 170C. The reaction product is recrystallized from petroleum ether at 100/120C and decolourized with decolourizing earth. 4-(p-dimethylamino-benzoyloxy)-2,2,6,6-tetramethylpiperidine is obtained in form of a crystalline white substance with m.p. 137-139C and specific extinction (E:) - 992 at 312 nm.
  • 2
  • [ 2403-88-5 ]
  • [ 327056-62-2 ]
  • C15H21N3O [ No CAS ]
  • 3
  • [ 2403-88-5 ]
  • [ 2351-36-2 ]
  • bis(2,2,6,6-tetramethylpiperidine-4-yl)naphthalene-2,6-dicarboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
25.6% First Step A mixture of 2,2,6,6-tetramethyl-4-piperidinol (13.70 g, 87.12 mmol) and NaH (60%, 2.09 g, 87.09 mmol) was heated under reflux in THF for 2 hours. The resulting reaction mixture was cooled to -10 C. or lower, and then a THF solution of naphthalene-2,6-dichloride dicarboxylic acid (10 g, 39.51 mmol) was slowly added dropwise thereto while the mixture was maintained at the temperature. The resulting reaction mixture was stirred at room temperature for 1 hour, and then quenched with water. The resulting mixture was subjected to extraction with MTBE. Silica gel was added to organic layers combined, and then filtered off. A solvent was distilled off from the resulting solution to give bis(2,2,6,6-tetramethylpiperidine-4-yl)naphthalene-2,6-dicarboxylate (No. 8) (5 g, yield: 25.6%). 1H-NMR (δ ppm; CDCl3): 8.60 (s, 2H), 8.11 (dd, 2H), 8.00 (d, 2H), 5.52 (tt, 2H), 2.12 (dd, 4H), 1.55 (br, 2H), 1.37 (t, 4H), 1.32 (s, 12H), 1.22 (s, 12H).
 

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