Acetic acid (2R,3R)-3-hydroxy-3-(4-methoxy-phenyl)-2-methyl-propyl ester

Base Information

Chemical Name:Acetic acid (2R,3R)-3-hydroxy-3-(4-methoxy-phenyl)-2-methyl-propyl ester
CAS No.:262849-41-2
Molecular Formula:C₁₃H₁₈O₄
Molecular Weight:238.284
Hs Code.:

Synonyms:Acetic acid (2R,3R)-3-hydroxy-3-(4-methoxy-phenyl)-2-methyl-propyl ester

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Chemical Property of Acetic acid (2R,3R)-3-hydroxy-3-(4-methoxy-phenyl)-2-methyl-propyl ester

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Technology Process of Acetic acid (2R,3R)-3-hydroxy-3-(4-methoxy-phenyl)-2-methyl-propyl ester

There total 5 articles about Acetic acid (2R,3R)-3-hydroxy-3-(4-methoxy-phenyl)-2-methyl-propyl 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:

: 91970-30-8,139711-01-6,37542-82-8
(E)-3-(4-Methoxyphenyl)-2-methylprop-2-en-1-ol

: 262849-41-2
Acetic acid (2R,3R)-3-hydroxy-3-(4-methoxy-phenyl)-2-methyl-propyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: BH₃*Me₂S / tetrahydrofuran / 2 h / 20 °C

1.2: 89 percent / NaOH; 30 percent aq. H₂O₂ / tetrahydrofuran

2.1: lipase Amano P / 33 °C

With dimethylsulfide borane complex; lipase Amano P; In tetrahydrofuran;
DOI:10.1248/cpb.48.272

Reference yield:

: 17226-85-6,17226-86-7,34880-65-4,119068-85-8,136521-24-9,136521-25-0,136734-11-7
α,β-syn-methyl 3-hydroxy-2-methyl-3-(p-methoxyphenyl)propionate

: 262849-41-2
Acetic acid (2R,3R)-3-hydroxy-3-(4-methoxy-phenyl)-2-methyl-propyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 95 percent / methanesulfonic acid / CHCl₃ / 12 h / 20 °C

2.1: 90 percent / LiAlH₄ / tetrahydrofuran / 0.17 h / 20 °C

3.1: BH₃*Me₂S / tetrahydrofuran / 2 h / 20 °C

3.2: 89 percent / NaOH; 30 percent aq. H₂O₂ / tetrahydrofuran

4.1: lipase Amano P / 33 °C

With lithium aluminium tetrahydride; methanesulfonic acid; dimethylsulfide borane complex; lipase Amano P; In tetrahydrofuran; chloroform;
DOI:10.1248/cpb.48.272

Reference yield:

: 17226-85-6,17226-86-7,34880-65-4,119068-85-8,136521-24-9,136521-25-0,136734-11-7
α,β-anti-methyl 3-hydroxy-2-methyl-3-(p-methoxyphenyl)propionate

: 262849-41-2
Acetic acid (2R,3R)-3-hydroxy-3-(4-methoxy-phenyl)-2-methyl-propyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / LiAlH₄ / diethyl ether / 0.17 h / 20 °C

2: lipase Amano P / 33 °C

With lithium aluminium tetrahydride; lipase Amano P; In diethyl ether;
DOI:10.1248/cpb.48.272