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Chemical Structure| 51015-37-3 Chemical Structure| 51015-37-3

Structure of 51015-37-3

Chemical Structure| 51015-37-3

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Product Details of [ 51015-37-3 ]

CAS No. :51015-37-3
Formula : C14H18O
M.W : 202.29
SMILES Code : O=C1CCCC2=C1C=CC(C(C)(C)C)=C2
MDL No. :MFCD11518721

Safety of [ 51015-37-3 ]

Application In Synthesis of [ 51015-37-3 ]

* 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 [ 51015-37-3 ]

[ 51015-37-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 51015-37-3 ]
  • [ 80567-00-6 ]
  • 6-tert-butyl-2-cis-(2,6-dimethylmorpholinomethyl)-1,2,3,4-tetrahydronaphthalen-1-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
39% With paraformaldehyde;hydrogenchloride; In ethanol; water; EXAMPLE 3 This Example illustrates the preparation of 7-tert-butyl-3-cis-(2,6-dimethylmorpholinomethyl)-1,2-dihydronaphthalene (Compound No. 2 in Table I). 2,6-Dimethylmorpholine hydrochloride (12.1 g, 0.08 mol), 6-tert-butyl-1,2,3,4-tetrahydronaphthalen-1-one (8.1 g, 0.04 mol) and paraformaldehyde (2.4 g, 0.08 mol) were refluxed together in ethanol (150 ml) with concentrated hydrochloric acid (1 ml) as a catalyst for 16 hours. The reaction mixture was concentrated under reduced pressure and the residue dissolved in water then extracted with diethyl ether. The resulting aqueous solution was neutralised with sodium bicarbonate and extracted with diethyl ether (2*200 ml); the ethereal extracts were dried over anhydrous magnesium sulphate and concentrated under reduced pressure to give an orange oil. This oil was purified by hplc (silica eluted with ethyl acetate/petroleum ether 1:1) to give 6-tert-butyl-2-cis-(2,6-dimethylmorpholinomethyl)-1,2,3,4-tetrahydronaphthalen-1-one (5.1 g, 39%).
39% With paraformaldehyde;hydrogenchloride; In ethanol; water; EXAMPLE 2 This Example illustrates the preparation of 6-tert-butyl-2-cis-(2,6-dimethylmorpholinomethyl)-1,2,3,4-tetrahydronaphthalene (Compound No. 21 in Table I). 2,6-Dimethylmorpholine hydrochloride (12.1 g, 0.08 mol), 6-tert-butyl-1,2,3,4-tetrahydronaphthalen-1-one (8.1 g, 0.04 mol), and paraformaldehyde (2.4 g, 0.08 mol) were refluxed together in ethanol (150 ml) with concentrated hydrochloric acid (1 ml) as a catalyst for 16 hours. The reaction mixture was concentrated under reduced pressure and the residue dissolved in water then extracted with diethyl ether. The resulting aqueous solution was neutralised with sodium bicarbonate and extracted with diethyl ether (2*200 ml); the ethereal extracts were dried over anhydrous magnesium sulphate and concentrated under reduced pressure to give an orange oil. This oil was purified by hplc (silica eluted with ethyl acetate/petroleum ether 1:1) to give 6-tert-butyl-2-cis-(2,6-dimethylmorpholinomethyl)-1,2,3,4-tetrahydronaphthalen-1-one (5.1 g, 39%).
 

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