<3R-<3α,5α(S^*)>>-8-methyl-3-(phenylmethoxy)-1-oxaspiro<4.5>dec-6-en-2-one

Base Information

Chemical Name:<3R-<3α,5α(S^*)>>-8-methyl-3-(phenylmethoxy)-1-oxaspiro<4.5>dec-6-en-2-one
CAS No.:143842-74-4
Molecular Formula:C₁₇H₂₀O₃
Molecular Weight:272.344
Hs Code.:

<3R-<3α,5α(S<sup>*</sup>)>>-8-methyl-3-(phenylmethoxy)-1-oxaspiro<4.5>dec-6-en-2-one

Synonyms:<3R-<3α,5α(S^*)>>-8-methyl-3-(phenylmethoxy)-1-oxaspiro<4.5>dec-6-en-2-one

Suppliers and Price of <3R-<3α,5α(S^*)>>-8-methyl-3-(phenylmethoxy)-1-oxaspiro<4.5>dec-6-en-2-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of <3R-<3α,5α(S^*)>>-8-methyl-3-(phenylmethoxy)-1-oxaspiro<4.5>dec-6-en-2-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of <3R-<3α,5α(S^*)>>-8-methyl-3-(phenylmethoxy)-1-oxaspiro<4.5>dec-6-en-2-one

There total 3 articles about <3R-<3α,5α(S^*)>>-8-methyl-3-(phenylmethoxy)-1-oxaspiro<4.5>dec-6-en-2-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:

: 81927-55-1
O-benzyl 2,2,2-trichloroacetimidate

: 143842-74-4
<3R-<3α,5α(S^*)>>-8-methyl-3-(phenylmethoxy)-1-oxaspiro<4.5>dec-6-en-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / CF₃SO₃H / CH₂Cl₂; cyclohexane / Ambient temperature

2: 1) aq. KOH, 2) I₂, KI, 3) 1,4-diazabicyclo<2.2.2>octane / 1) MeOH, r.t., 2) H₂O, hexane, EtOAc, r.t., 1 h, 3) DMSO, 132-140 deg C, 15 min

With 1,4-diaza-bicyclo[2.2.2]octane; potassium hydroxide; trifluorormethanesulfonic acid; iodine; potassium iodide; In dichloromethane; cyclohexane;
DOI:10.1021/jo00052a029

Reference yield:

: (R)-α-hydroxy-4-methyl-1-cyclohexene-1-propanoic acid methyl ester

: 143842-74-4
<3R-<3α,5α(S^*)>>-8-methyl-3-(phenylmethoxy)-1-oxaspiro<4.5>dec-6-en-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / CF₃SO₃H / CH₂Cl₂; cyclohexane / Ambient temperature

2: 1) aq. KOH, 2) I₂, KI, 3) 1,4-diazabicyclo<2.2.2>octane / 1) MeOH, r.t., 2) H₂O, hexane, EtOAc, r.t., 1 h, 3) DMSO, 132-140 deg C, 15 min

With 1,4-diaza-bicyclo[2.2.2]octane; potassium hydroxide; trifluorormethanesulfonic acid; iodine; potassium iodide; In dichloromethane; cyclohexane;
DOI:10.1021/jo00052a029

Reference yield:

: R-(α)-(phenylmethoxy)-4-methyl-1-cyclohexene-1-propanoic acid methyl ester

: 143900-89-4
(3R,5R,8R)-3-Benzyloxy-8-methyl-1-oxa-spiro[4.5]dec-6-en-2-one

: 143842-74-4
<3R-<3α,5α(S^*)>>-8-methyl-3-(phenylmethoxy)-1-oxaspiro<4.5>dec-6-en-2-one

Guidance literature:: With 1,4-diaza-bicyclo[2.2.2]octane; potassium hydroxide; iodine; potassium iodide; Yield given. Multistep reaction. Yields of byproduct given; 1) MeOH, r.t., 2) H₂O, hexane, EtOAc, r.t., 1 h, 3) DMSO, 132-140 deg C, 15 min;
DOI:10.1021/jo00052a029