4-Methoxycyclohexanon

4-Methoxycyclohexanon Suppliers list
Company Name: Wuhan EEChem Technologies Co., Ltd  Gold
Tel: 0711-3617768 13308685235
Email: lihongcai4360@sina.com
Company Name: Xi'an Kaimeike New Material Co., Ltd.  Gold
Tel: 13720451009 13720451009
Email: 13720451009@163.com
Company Name: Xi 'an billiton biological technology co., LTD  Gold
Tel: 029-88764766
Email: wang.yali@xatuochao.com
Company Name: Hubei Yihua New Materials Technology Co., Ltd.  Gold
Tel: 17754433341 18086038039
Email: 986173822@qq.com
Company Name: Shanghai Kangenbo Medical Technology Co., Ltd.  Gold
Tel: 400-1388-521 17510465506
Email: renhuirong@kangenbo.cn

4-Methoxycyclohexanon manufacturers

4-Methoxycyclohexanon Basic information
Product Name:4-Methoxycyclohexanon
Synonyms:4-Metho×ycyclohe×anone;4-Methoxycyclohexanon;p-Methoxycyclohexanone;Cyclohexanone, 4-methoxy-;4-Methoxycyclohexano;4-methoxycyclohexanone, 98%min;4-methoxycyclohexan-1-one - [M82414];4-Methoxycyclohexan-1-one
CAS:13482-23-0
MF:C7H12O2
MW:128.17
EINECS:1308068-626-2
Product Categories:Intermediates;Miscellaneous reagents
Mol File:13482-23-0.mol
4-Methoxycyclohexanon Structure
4-Methoxycyclohexanon Chemical Properties
Boiling point 189 ºC
density 0.98
refractive index 1.4560
Fp 69 ºC
storage temp. 2-8°C
solubility soluble in Chloroform, Ethyl Acetate, Methanol
form liquid
color Clear, pale yellow
InChIInChI=1S/C7H12O2/c1-9-7-4-2-6(8)3-5-7/h7H,2-5H2,1H3
InChIKeyXADCKKKOYZJNAR-UHFFFAOYSA-N
SMILESC1(=O)CCC(OC)CC1
Safety Information
HS Code 2914500090
MSDS Information
4-Methoxycyclohexanon Usage And Synthesis
Uses4-Methoxycyclohexanone is a substituted cyclohexanone used in the preparation of various organic compounds such as antitumor agents.
Synthesis
4-Methoxyphenol

150-76-5

4-Methoxycyclohexanon

13482-23-0

The general procedure for the synthesis of p-methoxycyclohexanone from p-hydroxyanisole is as follows: 7 g of palladium-carbon catalyst and 1 g of borax were added to an autoclave, followed by 150 g of methylcyclohexane and 100 g of p-hydroxyanisole. The reaction was slowly heated to 100 °C and hydrogen was introduced into the system until the pressure reached 1.0 MPa, and stirring was started. When the pressure dropped to 0.5 MPa, hydrogen was supplemented to 1.0 MPa, keeping the reaction pressure in the range of 0.7-1.0 MPa. Continuously monitor the hydrogen consumption, and after the hydrogen consumption stops for a period of time, take samples for reaction process monitoring. When the remaining amount of raw material is less than 1%, the reaction is judged to be complete. The reaction mixture was cooled to 30°C and filtered to remove the catalyst. The filtrate was evaporated to remove the solvent and subsequently distilled under reduced pressure to give 92 g of p-methoxycyclohexanone in 90% yield.

References[1] Patent: CN107827881, 2018, A. Location in patent: Paragraph 0034; 0035
[2] Patent: US5886232, 1999, A
[3] Tetrahedron Letters, 1994, vol. 35, # 39, p. 7151 - 7154
[4] Journal of Organic Chemistry, 1961, vol. 26, p. 2633 - 2640
[5] Tetrahedron, 1976, vol. 32, p. 2589 - 2594
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