(1R,3R,4S,7R)-7-(2-Benzyloxy-ethyl)-3-methyl-bicyclo[2.2.1]hept-5-en-2-one

Base Information

Chemical Name:(1R,3R,4S,7R)-7-(2-Benzyloxy-ethyl)-3-methyl-bicyclo[2.2.1]hept-5-en-2-one
CAS No.:83061-01-2
Molecular Formula:C₁₇H₂₀O₂
Molecular Weight:256.345
Hs Code.:

Synonyms:(1R,3R,4S,7R)-7-(2-Benzyloxy-ethyl)-3-methyl-bicyclo[2.2.1]hept-5-en-2-one

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Chemical Property of (1R,3R,4S,7R)-7-(2-Benzyloxy-ethyl)-3-methyl-bicyclo[2.2.1]hept-5-en-2-one

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Technology Process of (1R,3R,4S,7R)-7-(2-Benzyloxy-ethyl)-3-methyl-bicyclo[2.2.1]hept-5-en-2-one

There total 5 articles about (1R,3R,4S,7R)-7-(2-Benzyloxy-ethyl)-3-methyl-bicyclo[2.2.1]hept-5-en-2-one 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: 74.0%

: 83061-00-1
(1R,4S,7R)-7-(2-Benzyloxy-ethyl)-bicyclo[2.2.1]hept-5-en-2-one

: 74-88-4
methyl iodide

: 83061-01-2
(1R,3R,4S,7R)-7-(2-Benzyloxy-ethyl)-3-methyl-bicyclo[2.2.1]hept-5-en-2-one

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃;
DOI:10.1021/ja00385a038

Reference yield:

: 100-44-7
benzyl chloride

: 83061-01-2
(1R,3R,4S,7R)-7-(2-Benzyloxy-ethyl)-3-methyl-bicyclo[2.2.1]hept-5-en-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: NaH / benzene; dimethylsulfoxide / 50 °C

2: 10percent HCl / tetrahydrofuran

3: 74 percent / LDA / tetrahydrofuran / -78 °C

With hydrogenchloride; sodium hydride; lithium diisopropyl amide; In tetrahydrofuran; dimethyl sulfoxide; benzene;
DOI:10.1021/ja00385a038

Reference yield:

: 83060-99-5
C₁₁H₁₆O₃

: 83061-01-2
(1R,3R,4S,7R)-7-(2-Benzyloxy-ethyl)-3-methyl-bicyclo[2.2.1]hept-5-en-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: NaH / benzene; dimethylsulfoxide / 50 °C

2: 10percent HCl / tetrahydrofuran

3: 74 percent / LDA / tetrahydrofuran / -78 °C

With hydrogenchloride; sodium hydride; lithium diisopropyl amide; In tetrahydrofuran; dimethyl sulfoxide; benzene;
DOI:10.1021/ja00385a038