N-tert-Butyl(benzoyloxy)acetamide

Base Information

Chemical Name:N-tert-Butyl(benzoyloxy)acetamide
CAS No.:106231-52-1
Molecular Formula:C13H17NO3
Molecular Weight:235.283
Hs Code.:
DSSTox Substance ID:DTXSID80872106
Nikkaji Number:J1.553.237H
ChEMBL ID:CHEMBL139033

Synonyms:106231-52-1;CHEMBL139033;DTXSID80872106;N-tert-Butyl(benzoyloxy)acetamide;Benzoic acid tert-butylcarbamoyl-methyl ester;2-[(2-Methyl-2-propanyl)amino]-2-oxoethyl benzoate

Suppliers and Price of N-tert-Butyl(benzoyloxy)acetamide

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 N-tert-Butyl(benzoyloxy)acetamide

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:235.12084340
Heavy Atom Count:17
Complexity:275

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)NC(=O)COC(=O)C1=CC=CC=C1

Technology Process of N-tert-Butyl(benzoyloxy)acetamide

There total 7 articles about N-tert-Butyl(benzoyloxy)acetamide 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: 70.0%

: 119072-55-8,7188-38-7
tert-butylisonitrile

: C₂₃H₂₀N₂O₂

: 106231-52-1
Benzoic acid tert-butylcarbamoyl-methyl ester

: 146495-24-1
N-(diphenylmethylene)aminoacetonitrile

Guidance literature:: With hydrogenchloride; iron(II) acetate; In 1,4-dioxane; water; at 90 ℃; for 48h; Inert atmosphere;
DOI:10.1039/d1cc03348d

Reference yield:

: 614-44-8
benzoyloxyacetic acid

: 106231-52-1
Benzoic acid tert-butylcarbamoyl-methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / SOCl₂ / 3 h / Heating

2: benzene / 1.5 h / Ambient temperature

With thionyl chloride; In benzene;
DOI:10.1002/jps.2600770402

Reference yield:

: 532-32-1
sodium benzoate

: 106231-52-1
Benzoic acid tert-butylcarbamoyl-methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / NaI / H₂O / 6 h / 90 °C

2: 80 percent / aq. HCl / 0.17 h / 75 °C

3: 88 percent / SOCl₂ / 3 h / Heating

4: benzene / 1.5 h / Ambient temperature

With hydrogenchloride; thionyl chloride; sodium iodide; In water; benzene;
DOI:10.1002/jps.2600770402