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Chemical Structure| 648921-37-3 Chemical Structure| 648921-37-3

Structure of 648921-37-3

Chemical Structure| 648921-37-3

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Product Details of [ 648921-37-3 ]

CAS No. :648921-37-3
Formula : C7H14ClNO
M.W : 163.65
SMILES Code : O=C1C(C)(C)CNCC1.[H]Cl
MDL No. :MFCD11043097
InChI Key :YKKXZGNFWDQKGO-UHFFFAOYSA-N
Pubchem ID :57358418

Safety of [ 648921-37-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 648921-37-3 ]

* 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 [ 648921-37-3 ]

[ 648921-37-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 648921-37-3 ]
  • [ 501-53-1 ]
  • [ 473838-66-3 ]
YieldReaction ConditionsOperation in experiment
78.5% With sodium hydrogencarbonate; In tetrahydrofuran; water; at 0 - 15℃; for 12h; Sodium bicarbonate (1.28 g, 15.28 mmol, 2.50 eq) and CbzCl (1.25 g, 7.33 mmol, 1.20 eq) was added to a mixed solution of 3,3-dimethylpiperidin-4-one; hydrochloride (1.00 g, 6.11 mmol, 1.00 eq) in tetrahydrofuran (5.00 mL) and water (5.00 mL) at 0 C. The mixture was stirred at 15 C for 12 hours. The reaction mixture was extracted with ethyl acetate (20 mL). The combined organic layers were washed with brine (10 mL * 2), dried over sodium sulfate, filtered and concentrated under reduced pressure to deliver benzyl 3,3-dimethyl-4-oxopiperidine-1-carboxylate (1.60 g, 4.81 mmol, 78.66% yield, 78.5% purity) as a colorless oil. 1H NMR (400MHz, CDCl3) delta 7.35-7.25 (m, 6H), 5.11 (s, 2H), 3.72 (t, J = 6.3 Hz, 2H), 3.42 (br. s., 2H), 2.44 (br. s., 2H), 1.02 (br. s., 6H).
With triethylamine; In dichloromethane; at 0 - 20℃; for 16h; Preparation of 1-66: A solution of 1-65 (4.20 g, 33.07 mmol) in CH2C12 (80 mL) was charged with benzyl chloroformate (6.70 g, 39.68 mmol) followed by triethyl amine (5.00 g, 49 mmol) over 20 min at 0C. The reaction mixture was stirred at RT for 16 h. The organic layer was washed with saturated NaHCC solution (50 mL), water (100 mL) and brine (50 mL). The organic layer was concentrated under reduced pressure to afford 1-66 as a liquid. MS (MM) m/z 262.1 [M + H]+.
5.80 g With potassium carbonate; In tetrahydrofuran; water; at 0 - 25℃; To a solution of 3,3-dimethylpiperidin-4-one hydrochloride (3.6 g, 22.0 mmol, 22.0 mL) in THF (22 mL) was added K2C03 (3 M, 14.6 mL) dissolved in H20 (15 mL). Then the mixture was cooled to 0 C and benzyl chloroformate (4.13 g, 24.2 mmol) was added dropwise. The reaction was stirred at 25 C for 2 h. The residue was poured into water (50 mL), extracted with EtOAc (50 mLx2). The combined organic layer was concentrated as a yellow liquid to afford benzyl 3,3- dimethyl-4-oxo-piperidine-l-carboxylate (5.80 g, 21.09 mmol, 96 % yield). MS (ES+) Ci5Hi9N03 requires: 261, found: 262 [M+H]+. 1H MR (400 MHz, MeOH-d4) delta: 7.42 - 7.35 (m, 5H), 5.19 (s, 2H), 3.78 (s, 2H), 3.53 (s, 2H), 2.50 (t, J= 6.5, 2H), 1.06 (s, 6H).
 

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