HCID 178478985, compound → HCID 19857657, compound
Reaction equation
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]#[C:9][Mg]Cl>O1CCCC1>[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]#[C:9][CH2:2]/[CH:3]=[CH:4]/[CH3:5]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The experimental procedure was substantially the same as in Example 1 except that the starting Grignard mixture contained 3 moles of 8-bromo-1-octynyl magnesium chloride in tetrahydrofuran in place of 8-chloro-1-octynyl magnesium chloride to give 529 g of 1-bromo-(E)-10-dodecen-7-yne in a purity of 95%. The yield was 69% of the theoretical value. Partial hydrogenation of 150.5 g of this ene-yne compound in the same manner as in Example 1 gave 145 g of a product boiling at 106° to 110° C. under a pressure of 1 mmHg, which could be identified by analysis to be 1-bromo-(Z,E)-7,10-dodecadiene. The analytical data leading to the identification of this product compound were as follows.
Sources & evidence
- ORD record
- ord-c7302a4952eb42c99c9f5bffb35ca019
- Source dataset
- uspto-grants-1990_04
- Patent number
- US04918252
Reaction notes
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