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3-chloro-5-<(E)-3,7-dimethyl-2,6-octadienyl>-4,6-dimethoxy-2-methylbenzyl alcohol

Base Information
  • Chemical Name:3-chloro-5-<(E)-3,7-dimethyl-2,6-octadienyl>-4,6-dimethoxy-2-methylbenzyl alcohol
  • CAS No.:157826-54-5
  • Molecular Formula:C20H29ClO3
  • Molecular Weight:352.901
  • Hs Code.:
3-chloro-5-<(E)-3,7-dimethyl-2,6-octadienyl>-4,6-dimethoxy-2-methylbenzyl alcohol

Synonyms:3-chloro-5-<(E)-3,7-dimethyl-2,6-octadienyl>-4,6-dimethoxy-2-methylbenzyl alcohol

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Chemical Property of 3-chloro-5-<(E)-3,7-dimethyl-2,6-octadienyl>-4,6-dimethoxy-2-methylbenzyl alcohol
Chemical Property:
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Technology Process of 3-chloro-5-<(E)-3,7-dimethyl-2,6-octadienyl>-4,6-dimethoxy-2-methylbenzyl alcohol

There total 6 articles about 3-chloro-5-<(E)-3,7-dimethyl-2,6-octadienyl>-4,6-dimethoxy-2-methylbenzyl alcohol 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:
Guidance literature:
Multi-step reaction with 4 steps
1: 97 percent / SO2Cl2 / diethyl ether / 3.5 h / Ambient temperature
2: 1.41 g / K2CO3 / acetone / 2.5 h / Heating
3: 1.) BuLi, 2.) CuCC-C(OMe)Me2 / 1.) hexane, THF, HMPA, -78 deg C, 30 min, 2.) 18 h -> room temperature
4: LiAlH4 / diethyl ether / 0 °C
With lithium aluminium tetrahydride; n-butyllithium; sulfuryl dichloride; potassium carbonate; In diethyl ether; acetone;
DOI:10.1246/bcsj.67.1178
Guidance literature:
Multi-step reaction with 3 steps
1: 1.41 g / K2CO3 / acetone / 2.5 h / Heating
2: 1.) BuLi, 2.) CuCC-C(OMe)Me2 / 1.) hexane, THF, HMPA, -78 deg C, 30 min, 2.) 18 h -> room temperature
3: LiAlH4 / diethyl ether / 0 °C
With lithium aluminium tetrahydride; n-butyllithium; potassium carbonate; In diethyl ether; acetone;
DOI:10.1246/bcsj.67.1178
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