(2S,3R)-3-Methyl-2-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexanoic acid methyl ester

Base Information

Chemical Name:(2S,3R)-3-Methyl-2-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexanoic acid methyl ester
CAS No.:76713-41-2
Molecular Formula:C₁₈H₂₃F₃O₅
Molecular Weight:376.373
Hs Code.:

Synonyms:(2S,3R)-3-Methyl-2-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexanoic acid methyl ester

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Chemical Property of (2S,3R)-3-Methyl-2-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexanoic acid methyl ester

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Technology Process of (2S,3R)-3-Methyl-2-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexanoic acid methyl ester

There total 7 articles about (2S,3R)-3-Methyl-2-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexanoic 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:

: 60182-96-9
2-amino-3-methylhexanoic acid

: 76713-41-2
(2S,3R)-3-Methyl-2-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 50 percent / acetic acid / 0.08 h / Heating

2: 55 percent / NaOH, Aspergillus acylase, CoCl₂ / H₂O / 96 h / 37 °C / pH = 6.7 to 6.8

3: 66 percent / NaNO₂, 1.5N H₂SO₄ / H₂O / 1.) 0-5 deg C, 1 h; 2.) 0-30 deg C, 2h

With sodium hydroxide; Aspergillus acylase; sulfuric acid; sodium nitrite; In water; acetic acid;
DOI:10.1016/0040-4020(80)80113-X

Reference yield:

: 123-15-9
2-methylvaleraldehyde

: 76713-41-2
(2S,3R)-3-Methyl-2-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: NH₄Cl, conc NH₃ aq / H₂O / 2 h / 0 - 20 °C

2: conc. HCl / 15 h / Heating

3: 50 percent / acetic acid / 0.08 h / Heating

4: 55 percent / NaOH, Aspergillus acylase, CoCl₂ / H₂O / 96 h / 37 °C / pH = 6.7 to 6.8

5: 66 percent / NaNO₂, 1.5N H₂SO₄ / H₂O / 1.) 0-5 deg C, 1 h; 2.) 0-30 deg C, 2h

With hydrogenchloride; ammonium hydroxide; sodium hydroxide; Aspergillus acylase; sulfuric acid; ammonium chloride; sodium nitrite; In water; acetic acid;
DOI:10.1016/0040-4020(80)80113-X

Reference yield:

: 28116-85-0
(2S,3R)-threo-2-amino-3-methylhexanoic acid

: 76713-41-2
(2S,3R)-3-Methyl-2-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 66 percent / NaNO₂, 1.5N H₂SO₄ / H₂O / 1.) 0-5 deg C, 1 h; 2.) 0-30 deg C, 2h

With sulfuric acid; sodium nitrite; In water;
DOI:10.1016/0040-4020(80)80113-X