Basic information Safety Supplier Related

TERT-BUTYL 4-OXOCYCLOHEXANECARBOXYLATE

Basic information Safety Supplier Related

TERT-BUTYL 4-OXOCYCLOHEXANECARBOXYLATE Basic information

Product Name:
TERT-BUTYL 4-OXOCYCLOHEXANECARBOXYLATE
Synonyms:
  • Cyclohexanecarboxylic acid, 4-oxo-, 1,1-dimethylethyl ester
  • tert-butyl 4-oxocyclohexane-1-carboxylate
  • 4-Boc-cyclohexanone
CAS:
38446-95-6
MF:
C11H18O3
MW:
198.26
Product Categories:
  • Drug Intermediates
Mol File:
38446-95-6.mol
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TERT-BUTYL 4-OXOCYCLOHEXANECARBOXYLATE Chemical Properties

Boiling point:
271.5±33.0 °C(Predicted)
Density 
1.042±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
Appearance
White to off-white Solid
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Safety Information

HS Code 
2914500090
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TERT-BUTYL 4-OXOCYCLOHEXANECARBOXYLATE Usage And Synthesis

Synthesis

874-61-3

75-65-0

38446-95-6

General procedure for the synthesis of tert-butyl 4-oxocyclohexanecarboxylate from 4-cyclohexanonecarboxylic acid and tert-butanol: To an ice-cold solution of Intermediate 7 (4-cyclohexanonecarboxylic acid, 5.0 g, 35 mmol) in pyridine (19 mL) and tert-butanol (27 mL) was added triclophosphorus oxychloride (POCl3, 4.7 mL, 50.6 mmol) dropwise. The reaction mixture was slowly warmed to room temperature and stirred continuously for 4 hours. Upon completion of the reaction, the crude reaction mixture was carefully poured into ice water and extracted with ethyl acetate (EtOAc). The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure to afford Intermediate 8 (tert-butyl 4-oxocyclohexanecarboxylate, 4.0 g, 58% yield), which could be used in the next reaction without further purification. The product was confirmed by 1H NMR (400 MHz, CDCl3): δ 2.66 (tt, J = 9.6, 3.9 Hz, 1H), 2.48 (dt, J = 14.8, 5.4 Hz, 2H), 2.36 (m, 2H), 2.18 (ddd, J = 14.1, 8.7, 4.4 Hz, 2H), 2.01 (dtd, J = 14.4, 9.5, 4.8 Hz, 2H), 1.48 (s, 9H). lC/MS analysis showed a calculated value of 198.3 for m/z and a measured value of 199.1 (M + 1)+.

References

[1] Biological and Pharmaceutical Bulletin, 1995, vol. 18, # 3, p. 407 - 410
[2] Patent: WO2017/17609, 2017, A1. Location in patent: Paragraph 00215
[3] Patent: WO2017/51355, 2017, A1. Location in patent: Paragraph 00217
[4] Patent: WO2013/163279, 2013, A1. Location in patent: Paragraph 00382

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