(E)-(R)-2-methoxymethoxymethyl-2-methyl-5-phenylpent-4-enoic acid methyl ester

Base Information

Chemical Name:(E)-(R)-2-methoxymethoxymethyl-2-methyl-5-phenylpent-4-enoic acid methyl ester
CAS No.:890027-72-2
Molecular Formula:C₁₆H₂₂O₄
Molecular Weight:278.348
Hs Code.:

Synonyms:(E)-(R)-2-methoxymethoxymethyl-2-methyl-5-phenylpent-4-enoic acid methyl ester

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Chemical Property of (E)-(R)-2-methoxymethoxymethyl-2-methyl-5-phenylpent-4-enoic acid methyl ester

Chemical Property:

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Technology Process of (E)-(R)-2-methoxymethoxymethyl-2-methyl-5-phenylpent-4-enoic acid methyl ester

There total 6 articles about (E)-(R)-2-methoxymethoxymethyl-2-methyl-5-phenylpent-4-enoic acid methyl ester 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:

: 189884-53-5
2-methyl-2-(3-phenyl-2-propenyl)malonic acid dimethyl ester

: 890027-72-2
(E)-(R)-2-methoxymethoxymethyl-2-methyl-5-phenylpent-4-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: PLE; phosphate buffer / 30 °C / pH 8

2: oxalyl chloride; DMF / CH₂Cl₂ / 20 °C

3: 16.21 g / NaBH₄ / tetrahydrofuran; methanol / 1.5 h / -30 °C

4: 99 percent / NaI; DIPEA / CH₂Cl₂ / Heating

With sodium tetrahydroborate; phosphate buffer; oxalyl dichloride; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; sodium iodide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ol060437x

Reference yield:

: 890027-41-5
(R)-2-methyl-2-(3-phenyl-2-propenyl)malonic acid monomethyl ester

: 890027-72-2
(E)-(R)-2-methoxymethoxymethyl-2-methyl-5-phenylpent-4-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: oxalyl chloride; DMF / CH₂Cl₂ / 20 °C

2: 16.21 g / NaBH₄ / tetrahydrofuran; methanol / 1.5 h / -30 °C

3: 99 percent / NaI; DIPEA / CH₂Cl₂ / Heating

With sodium tetrahydroborate; oxalyl dichloride; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; sodium iodide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ol060437x

Reference yield:

: (E)-(S)-2-Chlorocarbonyl-2-methyl-5-phenyl-pent-4-enoic acid methyl ester

: 890027-72-2
(E)-(R)-2-methoxymethoxymethyl-2-methyl-5-phenylpent-4-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 16.21 g / NaBH₄ / tetrahydrofuran; methanol / 1.5 h / -30 °C

2: 99 percent / NaI; DIPEA / CH₂Cl₂ / Heating

With sodium tetrahydroborate; N-ethyl-N,N-diisopropylamine; sodium iodide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ol060437x