1-Methoxy-4-{(S)-1-[(1R,2R)-2-(2-methoxy-ethoxymethoxymethyl)-cyclopentyl]-but-3-enyloxymethyl}-benzene

Base Information

Chemical Name:1-Methoxy-4-{(S)-1-[(1R,2R)-2-(2-methoxy-ethoxymethoxymethyl)-cyclopentyl]-but-3-enyloxymethyl}-benzene
CAS No.:768395-27-3
Molecular Formula:C₂₂H₃₄O₅
Molecular Weight:378.509
Hs Code.:

Synonyms:1-Methoxy-4-{(S)-1-[(1R,2R)-2-(2-methoxy-ethoxymethoxymethyl)-cyclopentyl]-but-3-enyloxymethyl}-benzene

Suppliers and Price of 1-Methoxy-4-{(S)-1-[(1R,2R)-2-(2-methoxy-ethoxymethoxymethyl)-cyclopentyl]-but-3-enyloxymethyl}-benzene

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 1-Methoxy-4-{(S)-1-[(1R,2R)-2-(2-methoxy-ethoxymethoxymethyl)-cyclopentyl]-but-3-enyloxymethyl}-benzene

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-Methoxy-4-{(S)-1-[(1R,2R)-2-(2-methoxy-ethoxymethoxymethyl)-cyclopentyl]-but-3-enyloxymethyl}-benzene

There total 9 articles about 1-Methoxy-4-{(S)-1-[(1R,2R)-2-(2-methoxy-ethoxymethoxymethyl)-cyclopentyl]-but-3-enyloxymethyl}-benzene 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: 93.0%

: 3970-21-6
2-Methoxyethoxymethyl chloride

: 768395-26-2
{(1R,2R)-2-[(S)-1-(4-Methoxy-benzyloxy)-but-3-enyl]-cyclopentyl}-methanol

: 768395-27-3
1-Methoxy-4-{(S)-1-[(1R,2R)-2-(2-methoxy-ethoxymethoxymethyl)-cyclopentyl]-but-3-enyloxymethyl}-benzene

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 25 ℃; for 8h;
DOI:10.1002/anie.200460203

Reference yield:

: 6453-07-2,28269-02-5,28269-03-6,35079-19-7,74500-50-8,115794-30-4
(+/-)-trans-4-oxo-1,2-cyclopentanedicarboxylic acid bis(methyl ester)

: 768395-27-3
1-Methoxy-4-{(S)-1-[(1R,2R)-2-(2-methoxy-ethoxymethoxymethyl)-cyclopentyl]-but-3-enyloxymethyl}-benzene

Guidance literature:: Multi-step reaction with 9 steps

1.1: 49 percent / pig liver esterase; phosphate buffer / H₂O / 1 h / pH 7.0

2.1: 72 percent / SnCl₄ / CH₂Cl₂ / 8 h / 0 - 25 °C

3.1: 92 percent / Raney Ni / methanol / 3 h / Heating

4.1: 92 percent / LiAlH₄ / diethyl ether / 12 h / 25 °C

5.1: 84 percent / imidazole; DMAP / CH₂Cl₂ / 8 h / 25 °C

6.1: 89 percent / Dess-Martin periodinane / CH₂Cl₂ / 1 h / 25 °C

7.1: toluene / 1 h / -78 °C

7.2: NaH / tetrahydrofuran / 1 h / 0 °C

7.3: TBAI / tetrahydrofuran / 12 h / 25 °C

8.1: 93 percent / TBAF / tetrahydrofuran / 12 h / 25 °C

9.1: 93 percent / iPr₂NEt / CH₂Cl₂ / 8 h / 0 - 25 °C

With 1H-imidazole; dmap; lithium aluminium tetrahydride; phosphate buffer; pig liver esterase; tetrabutyl ammonium fluoride; tin(IV) chloride; Dess-Martin periodane; N-ethyl-N,N-diisopropylamine; nickel; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; toluene; 6.1: Dess-Martin oxidation;
DOI:10.1002/anie.200460203

Reference yield:

: 35079-19-7
trans-(1R,2R)-1,2-Bis(methoxycarbonyl)-4-oxocyclopentane

: 768395-27-3
1-Methoxy-4-{(S)-1-[(1R,2R)-2-(2-methoxy-ethoxymethoxymethyl)-cyclopentyl]-but-3-enyloxymethyl}-benzene

Guidance literature:: Multi-step reaction with 8 steps

1.1: 72 percent / SnCl₄ / CH₂Cl₂ / 8 h / 0 - 25 °C

2.1: 92 percent / Raney Ni / methanol / 3 h / Heating

3.1: 92 percent / LiAlH₄ / diethyl ether / 12 h / 25 °C

4.1: 84 percent / imidazole; DMAP / CH₂Cl₂ / 8 h / 25 °C

5.1: 89 percent / Dess-Martin periodinane / CH₂Cl₂ / 1 h / 25 °C

6.1: toluene / 1 h / -78 °C

6.2: NaH / tetrahydrofuran / 1 h / 0 °C

6.3: TBAI / tetrahydrofuran / 12 h / 25 °C

7.1: 93 percent / TBAF / tetrahydrofuran / 12 h / 25 °C

8.1: 93 percent / iPr₂NEt / CH₂Cl₂ / 8 h / 0 - 25 °C

With 1H-imidazole; dmap; lithium aluminium tetrahydride; tetrabutyl ammonium fluoride; tin(IV) chloride; Dess-Martin periodane; N-ethyl-N,N-diisopropylamine; nickel; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; toluene; 5.1: Dess-Martin oxidation;
DOI:10.1002/anie.200460203