59499-36-4

Upstream product

• 64-17-5 ethanol 
• 7726-95-6 bromine 
• 78-79-5 isoprene 

Downstream Products

• 71687-02-0 (2E,4E)-3-Methyl-5-phenyl-penta-2,4-dien-1-ol 
• 105986-35-4 (2E,4E,6E,8E)-9-(6,6-Dimethyl-2-trifluoromethyl-cyclohex-1-enyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-ol 
• 68715-67-3 haagenolide 
• 36076-04-7 trans-retinylidene-n-butylamine 
• 116-31-4 all-trans-Retinal 
• 564-87-4 (11Z)-retinal 
• 111724-05-1 <(2E)-4-hydroxy-2-methyl-2-butenyl>triphenylphosphonium bromide 
• 205989-59-9 Toluene-4-sulfonic acid (E)-8-methyl-5-oxo-10-(tetrahydro-pyran-2-yloxy)-dec-8-enyl ester 
• 61976-12-3 (E)-2-((4-bromo-3-methylbut-2-en-1-yl)oxy)tetrahydro-2H-pyran 

Relevant academic research and scientific papers

A 4 - bromo -3 - methyl -2 - butene -1 - ethoxylate ester preparation method (by machine translation)

The invention discloses a 4 - bromo - 3 - methyl - 2 - butene - 1 - ethoxylate ester preparation method, comprises the following steps: the isoprene and water is continuously pumped into the filled with bromo succinimide of the 1st [...] reaction is performed in a reactor, by the 1st rectifying device to obtain the rectification product 4 - bromo - 3 - methyl - 2 - butene - 1 - ol and 1 - bromo - 2 - methyl - 3 - butene - 2 - ol; the rectification product and of acetic anhydride mixture is pumped into the filled with solid acid catalyst in the reactor 2nd esterification rearrangement reaction, to obtain a reaction solution; the reaction liquid is distilled under reduced pressure to recover the acetic acid and unreacted second grade acid anhydride, 2nd rectifying device obtained by 4 - bromo - 3 - methyl - 2 - butene - 1 - ethoxylate ester. The invention of 4 - bromo - 3 - methyl - 2 - butene - 1 - ethoxylate ester preparation method the product yield is high, it is easy to realize continuous, large-scale production. (by machine translation)