Technology Process of 2-Pentene, 1-chloro-, (Z)-
There total 1 articles about 2-Pentene, 1-chloro-, (Z)- 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:
-
With
metathesis catalyst;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 41 percent / copper / aq. KOH / 1.) 0 degC, 1 h, 2.) R.T. 3.5 h
2: 82 percent / 1.) triphenylphosphine, bromine, triethylamine / benzene / 1.) 0 degC, 2.) R.T. 4 h
3: 93 percent / diethyl ether / 1.) -78 degC, 10 min., 2.) 0 degC, 1 h
With
bromine; copper; triethylamine; triphenylphosphine;
In
potassium hydroxide; diethyl ether; benzene;
DOI:10.1139/v82-185
-
-
1211-29-6,20073-13-6,39924-52-2,42536-97-0,53369-26-9,62653-86-5,78609-06-0,93452-02-9,95722-42-2,109959-42-4,136233-36-8
methyl jasmonate
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 1) NaH / 1) allylalcohol, mineral oil, 90 deg C, 3 h; 2) 100 deg C, 3-4 h
2: 55 percent Chromat. / Pd(OAc)2, bis(diphenylphosphino)ethane / acetonitrile / Heating
3: NaOMe / methanol / 10 h / 0 °C
4: 90 percent / adipic acid / 6 h / 190 °C
With
palladium diacetate; Adipic acid; sodium methylate; sodium hydride; 1,2-bis-(diphenylphosphino)ethane;
In
methanol; acetonitrile;
DOI:10.1016/S0040-4020(01)83449-9