trans-4-Acetamidocyclopent-2-enemethyl Acetate

Base Information

Chemical Name:trans-4-Acetamidocyclopent-2-enemethyl Acetate
CAS No.:77745-30-3
Molecular Formula:C₁₀H₁₅NO₃
Molecular Weight:197.234
Hs Code.:

Synonyms:

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

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Chemical Property of trans-4-Acetamidocyclopent-2-enemethyl Acetate

Chemical Property:

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Technology Process of trans-4-Acetamidocyclopent-2-enemethyl Acetate

There total 5 articles about trans-4-Acetamidocyclopent-2-enemethyl Acetate 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:

: 61865-62-1
cis-4-aminocyclopent-2-nene-1-carboxylic acid hydrochloride

: 77745-30-3,86252-77-9
trans-4-Acetamidocyclopent-2-enemethyl Acetate

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / HCl / methanol / 1 h / Heating

2: 2.) 1N methanolic HCl / 1.) pH 10-11, 30 min; 2.) MeOH, reflux, 30 min

3: 93 percent / Lithium triethylborohydride / tetrahydrofuran / 0.5 h / 0 °C

4: pyridine

With hydrogenchloride; lithium triethylborohydride; In tetrahydrofuran; pyridine; methanol;
DOI:10.1021/jo00329a026

Reference yield:

: 77745-26-7,426226-35-9
Methyl trans-4-Aminocyclopent-2-enecarboxylate Hydrochloride

: 77745-30-3,86252-77-9
trans-4-Acetamidocyclopent-2-enemethyl Acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / Lithium triethylborohydride / tetrahydrofuran / 0.5 h / 0 °C

2: pyridine

With lithium triethylborohydride; In tetrahydrofuran; pyridine;
DOI:10.1021/jo00329a026

Reference yield:

: 77745-25-6,426226-35-9
cis-4-amino-2-cyclopentenecarboxylic acid methyl ester hydrochloride

: 77745-30-3,86252-77-9
trans-4-Acetamidocyclopent-2-enemethyl Acetate

Guidance literature:: Multi-step reaction with 3 steps

1: 2.) 1N methanolic HCl / 1.) pH 10-11, 30 min; 2.) MeOH, reflux, 30 min

2: 93 percent / Lithium triethylborohydride / tetrahydrofuran / 0.5 h / 0 °C

3: pyridine

With hydrogenchloride; lithium triethylborohydride; In tetrahydrofuran; pyridine;
DOI:10.1021/jo00329a026