(R)-2-[(S)-1-(4-Methoxy-phenyl)-but-3-enyloxy]-propionic acid ethyl ester

Base Information

Chemical Name:(R)-2-[(S)-1-(4-Methoxy-phenyl)-but-3-enyloxy]-propionic acid ethyl ester
CAS No.:265641-91-6
Molecular Formula:C₁₆H₂₂O₄
Molecular Weight:278.348
Hs Code.:

Synonyms:(R)-2-[(S)-1-(4-Methoxy-phenyl)-but-3-enyloxy]-propionic acid ethyl ester

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Chemical Property of (R)-2-[(S)-1-(4-Methoxy-phenyl)-but-3-enyloxy]-propionic acid ethyl ester

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Technology Process of (R)-2-[(S)-1-(4-Methoxy-phenyl)-but-3-enyloxy]-propionic acid ethyl ester

There total 1 articles about (R)-2-[(S)-1-(4-Methoxy-phenyl)-but-3-enyloxy]-propionic acid ethyl 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:

: 24165-60-4,106650-97-9,132587-13-4,115413-90-6
(S)-1-(4-methoxyphenyl)but-3-en-1-ol

: 535-11-5,41978-69-2
Ethyl 2-bromopropionate

: 265641-91-6
(R)-2-[(S)-1-(4-Methoxy-phenyl)-but-3-enyloxy]-propionic acid ethyl ester

: 265641-84-7
(S)-2-[(S)-1-(4-Methoxy-phenyl)-but-3-enyloxy]-propionic acid ethyl ester

Guidance literature:: With sodium hydride; In tetrahydrofuran;
DOI:10.1021/ol005522y

Reference yield: 85.0%

: 265641-91-6
(R)-2-[(S)-1-(4-Methoxy-phenyl)-but-3-enyloxy]-propionic acid ethyl ester

: 265641-92-7
(R)-2-[(S)-1-(4-Methoxy-phenyl)-but-3-enyloxy]-propionaldehyde

Guidance literature:: With diisobutylaluminium hydride;
DOI:10.1021/ol005522y

Reference yield:

: 265641-91-6
(R)-2-[(S)-1-(4-Methoxy-phenyl)-but-3-enyloxy]-propionic acid ethyl ester

: (2R,3S,4R,6R)-6-(4-Methoxy-phenyl)-2-methyl-tetrahydro-pyran-3,4-diol

Guidance literature:: Multi-step reaction with 6 steps

1: 85 percent / DIBAL-H

2: 53 percent

3: 92 percent / Grubbs' catalyst

4: MCPBA

5: BF₃*OEt₂

6: 85 percent / K₂CO₃ / methanol

With boron trifluoride diethyl etherate; diisobutylaluminium hydride; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; Grubbs catalyst first generation; In methanol; 1: Reduction / 2: Wittig reaction / 3: Cyclization / 4: Oxidation / 5: Ring cleavage / 6: Deacetylation;
DOI:10.1021/ol005522y