3-Isopropyl-1-(3-methoxymethoxymethyl-2-methyl-phenyl)-4-methyl-pent-4-en-1-one

Base Information

Chemical Name:3-Isopropyl-1-(3-methoxymethoxymethyl-2-methyl-phenyl)-4-methyl-pent-4-en-1-one
CAS No.:218765-82-3
Molecular Formula:C₁₉H₂₈O₃
Molecular Weight:304.43
Hs Code.:

Synonyms:3-Isopropyl-1-(3-methoxymethoxymethyl-2-methyl-phenyl)-4-methyl-pent-4-en-1-one

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Chemical Property of 3-Isopropyl-1-(3-methoxymethoxymethyl-2-methyl-phenyl)-4-methyl-pent-4-en-1-one

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Technology Process of 3-Isopropyl-1-(3-methoxymethoxymethyl-2-methyl-phenyl)-4-methyl-pent-4-en-1-one

There total 9 articles about 3-Isopropyl-1-(3-methoxymethoxymethyl-2-methyl-phenyl)-4-methyl-pent-4-en-1-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 218765-80-1
3-Isopropyl-1-(3-methoxymethoxymethyl-2-methyl-phenyl)-4-methyl-pent-4-en-1-ol

: 218765-82-3
3-Isopropyl-1-(3-methoxymethoxymethyl-2-methyl-phenyl)-4-methyl-pent-4-en-1-one

Guidance literature:: With N-methyl-2-indolinone; tetrapropylammonium perruthennate; In dichloromethane; at 0 - 22 ℃; Yield given;
DOI:10.1016/S0040-4039(98)01965-0

Reference yield:

: 1975-50-4
2-methyl-3-nitrobenzic acid

: 218765-82-3
3-Isopropyl-1-(3-methoxymethoxymethyl-2-methyl-phenyl)-4-methyl-pent-4-en-1-one

Guidance literature:: Multi-step reaction with 6 steps

1: H₂ / Pd/C / dimethylformamide / 2223.7 Torr

2: 1.) NaNO₂, HCl; 2.) KI / 1.) DMF

3: 83 percent / BH₃*SMe₂, B(OMe)3 / tetrahydrofuran / 20 °C

4: 97 percent / i-Pr₂NEt / CH₂Cl₂ / 0 - 20 °C

5: t-BuLi / tetrahydrofuran

6: TPAP, NMO / CH₂Cl₂ / 0 - 22 °C

With hydrogenchloride; N-methyl-2-indolinone; tetrapropylammonium perruthennate; Trimethyl borate; dimethylsulfide borane complex; hydrogen; tert.-butyl lithium; N-ethyl-N,N-diisopropylamine; potassium iodide; sodium nitrite; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(98)01965-0

Reference yield:

: 13979-26-5
ethyl 2,4-dimethyl-2-pentenoate

: 218765-82-3
3-Isopropyl-1-(3-methoxymethoxymethyl-2-methyl-phenyl)-4-methyl-pent-4-en-1-one

Guidance literature:: Multi-step reaction with 4 steps

1: 87 percent / LAH / diethyl ether / 0 °C

2: 69 percent / Hg(OAc)2 / 12 h / 200 °C / 7240.07 Torr

3: t-BuLi / tetrahydrofuran

4: TPAP, NMO / CH₂Cl₂ / 0 - 22 °C

With lithium aluminium tetrahydride; N-methyl-2-indolinone; tetrapropylammonium perruthennate; mercury(II) diacetate; tert.-butyl lithium; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1016/S0040-4039(98)01965-0