4--3-hydroxy-buttersaeureethylester

Base Information

Chemical Name:4--3-hydroxy-buttersaeureethylester
CAS No.:6728-42-3
Molecular Formula:C₁₉H₂₆O₃
Molecular Weight:302.414
Hs Code.:

4-<p-Cyclohepten-(1)-yl-phenyl>-3-hydroxy-buttersaeureethylester

Synonyms:

Suppliers and Price of 4--3-hydroxy-buttersaeureethylester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4--3-hydroxy-buttersaeureethylester

Chemical Property:

Purity/Quality:

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MSDS Files:

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Technology Process of 4--3-hydroxy-buttersaeureethylester

There total 4 articles about 4--3-hydroxy-buttersaeureethylester 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:

: 6732-11-2
3-(p-Cyclohepten-⁽¹⁾-ylphenyl)-2-hydroxy-propylchlorid

: 6728-42-3
4--3-hydroxy-buttersaeureethylester

Guidance literature:: Multi-step reaction with 2 steps

1: aq. ethanol / Heating

2: HCl / Heating

With hydrogenchloride; In ethanol;
DOI:10.1021/jm00312a008

Reference yield:

: 6725-26-4
1-(4-bromophenyl)cycloheptene

: 6728-42-3
4--3-hydroxy-buttersaeureethylester

Guidance literature:: Multi-step reaction with 3 steps

1: (i) Mg, Et₂O, THF, (ii) /BRN= 79785/

2: aq. ethanol / Heating

3: HCl / Heating

With hydrogenchloride; In ethanol;
DOI:10.1021/jm00312a008

Reference yield:

: 502-42-1
cycloheptanone

: 6728-42-3
4--3-hydroxy-buttersaeureethylester

Guidance literature:: Multi-step reaction with 4 steps

1: (i) Mg, Et₂O, (ii) /BRN= 969823/, (iii) Ac₂O, AcOH

2: (i) Mg, Et₂O, THF, (ii) /BRN= 79785/

3: aq. ethanol / Heating

4: HCl / Heating

With hydrogenchloride; In ethanol;
DOI:10.1021/jm00312a008