ethyl 1-carbamoyl-1-cyclobutane carboxylate

Base Information

Chemical Name:ethyl 1-carbamoyl-1-cyclobutane carboxylate
CAS No.:219322-91-5
Molecular Formula:C₁₆H₂₁NO₃
Molecular Weight:275.348
Hs Code.:

ethyl 1-<N-1(R)-phenylethyl>carbamoyl-1-cyclobutane carboxylate

Synonyms:ethyl 1-carbamoyl-1-cyclobutane carboxylate

Suppliers and Price of ethyl 1-carbamoyl-1-cyclobutane carboxylate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of ethyl 1-carbamoyl-1-cyclobutane carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl 1-carbamoyl-1-cyclobutane carboxylate

There total 3 articles about ethyl 1-carbamoyl-1-cyclobutane carboxylate 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:

: 3779-29-1
diethyl cyclobutane-1,1-dicarboxylate

: 219322-91-5
ethyl 1-carbamoyl-1-cyclobutane carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / 10 percent aq. KOH / methanol / 18 h / Ambient temperature

2: Et₃N / CHCl₃ / 0.33 h / Ambient temperature

3: CHCl₃ / 0.5 h / Ambient temperature

With potassium hydroxide; triethylamine; In methanol; chloroform;
DOI:10.1248/cpb.46.1710

Reference yield:

: 54450-84-9
ethyl hydrogen cyclobutane-1,1-dicarboxylate

: 219322-91-5
ethyl 1-carbamoyl-1-cyclobutane carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CHCl₃ / 0.33 h / Ambient temperature

2: CHCl₃ / 0.5 h / Ambient temperature

With triethylamine; In chloroform;
DOI:10.1248/cpb.46.1710