<5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadien-1-yl>triphenylphosphonium bromide

Base Information

Chemical Name:<5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadien-1-yl>triphenylphosphonium bromide
CAS No.:79734-41-1
Molecular Formula:Br*C₃₃H₃₈OP
Molecular Weight:561.542
Hs Code.:

Synonyms:<5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadien-1-yl>triphenylphosphonium bromide

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Chemical Property of <5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadien-1-yl>triphenylphosphonium bromide

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Technology Process of <5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadien-1-yl>triphenylphosphonium bromide

There total 12 articles about <5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadien-1-yl>triphenylphosphonium bromide 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: 84.0%

: 79734-41-1
<5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadien-1-yl>triphenylphosphonium bromide

Guidance literature:

Reference yield:

: 95343-65-0
2-trans-5-(4'-hydroxy-2',2',6'-trimethylclohex-1'-enyl)-3-methylpent-2-en-4-yn-1-yltriphenylphosphonium bromide

: 79734-41-1
<5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadien-1-yl>triphenylphosphonium bromide

Guidance literature:: With hydrogen; barium sulfate; In methanol; palladium;

Reference yield:

: 28840-09-7
ethyl 5-(4,4-ehtylenedioxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadienoate

: 79734-41-1
<5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadien-1-yl>triphenylphosphonium bromide

Guidance literature:: Multi-step reaction with 3 steps

1: 62 percent / aq. 2N HCl, sodium cyanoborohydride / methanol

2: 54 mg / LiAlH₄ / diethyl ether / 0.5 h

3: methanol / 16 h / 20 °C

With hydrogenchloride; lithium aluminium tetrahydride; sodium cyanoborohydride; In methanol; diethyl ether;
DOI:10.1002/hlca.19810640414