4-methyl-5(R)-<1-(((1,1-dimethylethyl)dimethylsilyl)oxy)-2(R)-propyl>-3-cyclohexen-1-one

Base Information

Chemical Name:4-methyl-5(R)-<1-(((1,1-dimethylethyl)dimethylsilyl)oxy)-2(R)-propyl>-3-cyclohexen-1-one
CAS No.:112321-13-8
Molecular Formula:C₁₆H₃₀O₂Si
Molecular Weight:282.498
Hs Code.:

Synonyms:4-methyl-5(R)-<1-(((1,1-dimethylethyl)dimethylsilyl)oxy)-2(R)-propyl>-3-cyclohexen-1-one

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Chemical Property of 4-methyl-5(R)-<1-(((1,1-dimethylethyl)dimethylsilyl)oxy)-2(R)-propyl>-3-cyclohexen-1-one

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Technology Process of 4-methyl-5(R)-<1-(((1,1-dimethylethyl)dimethylsilyl)oxy)-2(R)-propyl>-3-cyclohexen-1-one

There total 15 articles about 4-methyl-5(R)-<1-(((1,1-dimethylethyl)dimethylsilyl)oxy)-2(R)-propyl>-3-cyclohexen-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:

: 112321-00-3,112419-70-2
2-((1R,5S)-5-Isopropenyl-2-methyl-cyclohex-2-enyl)-propan-1-ol

: 112321-13-8
4-methyl-5(R)-<1-(((1,1-dimethylethyl)dimethylsilyl)oxy)-2(R)-propyl>-3-cyclohexen-1-one

Guidance literature:: Multi-step reaction with 6 steps

1: 85 percent / N-bromosuccinimide / acetone / 0.25 h / 0 °C

2: O₃ / CH₂Cl₂ / 0.2 h / -78 °C

3: acetic anhydride, Et₃N, (N,N-dimethylamino)pyridine / CH₂Cl₂ / 16 h / 40 °C

4: 7 percent / zinc / ethanol; H₂O / 16 h / Heating

5: 83 percent / Et₃N, DMAP / CH₂Cl₂ / 15 h / Ambient temperature

6: 1.) oxalyl chloride, DMSO, Et₃N / 1.) CH₂Cl₂, -50 deg C, 15 min, 2.) a) -50 deg C, 5 min, b.) RT

With dmap; N-Bromosuccinimide; oxalyl dichloride; acetic anhydride; ozone; dimethyl sulfoxide; triethylamine; zinc; In ethanol; dichloromethane; water; acetone;
DOI:10.1021/jo00238a030

Reference yield:

: 112347-68-9
1-((3R,3aR,5R,7S,7aS)-7-Bromo-3,7a-dimethyl-octahydro-benzofuran-5-yl)-1-methoxy-eth-1-yl-hydroperoxide

: 112321-13-8
4-methyl-5(R)-<1-(((1,1-dimethylethyl)dimethylsilyl)oxy)-2(R)-propyl>-3-cyclohexen-1-one

Guidance literature:: Multi-step reaction with 4 steps

1: acetic anhydride, Et₃N, (N,N-dimethylamino)pyridine / CH₂Cl₂ / 16 h / 40 °C

2: 7 percent / zinc / ethanol; H₂O / 16 h / Heating

3: 83 percent / Et₃N, DMAP / CH₂Cl₂ / 15 h / Ambient temperature

4: 1.) oxalyl chloride, DMSO, Et₃N / 1.) CH₂Cl₂, -50 deg C, 15 min, 2.) a) -50 deg C, 5 min, b.) RT

With dmap; oxalyl dichloride; acetic anhydride; dimethyl sulfoxide; triethylamine; zinc; In ethanol; dichloromethane; water;
DOI:10.1021/jo00238a030

Reference yield:

: 112347-67-8
6(R)-1(S),7(R)-dimethyl-2(S)-bromo-4(R)-(2-propenyl)-9-oxabicyclo<4.3.0>nonane

: 112321-13-8
4-methyl-5(R)-<1-(((1,1-dimethylethyl)dimethylsilyl)oxy)-2(R)-propyl>-3-cyclohexen-1-one

Guidance literature:: Multi-step reaction with 5 steps

1: O₃ / CH₂Cl₂ / 0.2 h / -78 °C

2: acetic anhydride, Et₃N, (N,N-dimethylamino)pyridine / CH₂Cl₂ / 16 h / 40 °C

3: 7 percent / zinc / ethanol; H₂O / 16 h / Heating

4: 83 percent / Et₃N, DMAP / CH₂Cl₂ / 15 h / Ambient temperature

5: 1.) oxalyl chloride, DMSO, Et₃N / 1.) CH₂Cl₂, -50 deg C, 15 min, 2.) a) -50 deg C, 5 min, b.) RT

With dmap; oxalyl dichloride; acetic anhydride; ozone; dimethyl sulfoxide; triethylamine; zinc; In ethanol; dichloromethane; water;
DOI:10.1021/jo00238a030