1-[(Z)-(R)-1-(2,2-Dibromo-vinyl)-hex-3-enyloxymethyl]-4-methoxy-benzene

Base Information

Chemical Name:1-[(Z)-(R)-1-(2,2-Dibromo-vinyl)-hex-3-enyloxymethyl]-4-methoxy-benzene
CAS No.:164524-18-9
Molecular Formula:C₁₆H₂₀Br₂O₂
Molecular Weight:404.142
Hs Code.:

Synonyms:1-[(Z)-(R)-1-(2,2-Dibromo-vinyl)-hex-3-enyloxymethyl]-4-methoxy-benzene

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-[(Z)-(R)-1-(2,2-Dibromo-vinyl)-hex-3-enyloxymethyl]-4-methoxy-benzene

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Technology Process of 1-[(Z)-(R)-1-(2,2-Dibromo-vinyl)-hex-3-enyloxymethyl]-4-methoxy-benzene

There total 6 articles about 1-[(Z)-(R)-1-(2,2-Dibromo-vinyl)-hex-3-enyloxymethyl]-4-methoxy-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: 73.0%

: 558-13-4
carbon tetrabromide

: 164524-17-8
(R,Z)-2-[(4-methoxybenzyl)oxy]hept-4-enal

: 164524-18-9
1-[(Z)-(R)-1-(2,2-Dibromo-vinyl)-hex-3-enyloxymethyl]-4-methoxy-benzene

Guidance literature:: With triethylamine; triphenylphosphine; In dichloromethane; at 0 - 20 ℃; for 18h;
DOI:10.1021/jo962312j

Reference yield:

: 89238-99-3
O-(4-methoxybenzyl)-trichloroacetimidate

: 164524-18-9
1-[(Z)-(R)-1-(2,2-Dibromo-vinyl)-hex-3-enyloxymethyl]-4-methoxy-benzene

Guidance literature:: Multi-step reaction with 5 steps

1: 75 percent / TfOH / CH₂Cl₂; cyclohexane / 3 h / Ambient temperature; other reagent

2: 100 percent / DIBAL-H / toluene / -20 °C

3: 1.) THF, 0 deg C, 10 min; rt, 30 min, 2.) -78 deg C, 5 min; 0 deg C, 30 in

4: 96 percent / oxalyl chloride, DMSO / CH₂Cl₂ / 0.33 h / -78 °C

5: 73 percent / PPh₃, Et₃N / CH₂Cl₂ / 18 h / 0 - 20 °C

With oxalyl dichloride; trifluorormethanesulfonic acid; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; triphenylphosphine; In dichloromethane; cyclohexane; toluene;
DOI:10.1021/jo962312j

Reference yield:

: 194540-66-4
(S)-4-(4-Methoxy-benzyloxy)-tetrahydro-furan-2-ol

: 164524-18-9
1-[(Z)-(R)-1-(2,2-Dibromo-vinyl)-hex-3-enyloxymethyl]-4-methoxy-benzene

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) THF, 0 deg C, 10 min; rt, 30 min, 2.) -78 deg C, 5 min; 0 deg C, 30 in

2: 96 percent / oxalyl chloride, DMSO / CH₂Cl₂ / 0.33 h / -78 °C

3: 73 percent / PPh₃, Et₃N / CH₂Cl₂ / 18 h / 0 - 20 °C

With oxalyl dichloride; dimethyl sulfoxide; triethylamine; triphenylphosphine; In dichloromethane;
DOI:10.1021/jo962312j