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BETA-OXO-4-TERT-BUTYL-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER

Base Information Edit
  • Chemical Name:BETA-OXO-4-TERT-BUTYL-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER
  • CAS No.:545394-17-0
  • Molecular Formula:C17H24O3
  • Molecular Weight:276.376
  • Hs Code.:
  • Mol file:545394-17-0.mol
BETA-OXO-4-TERT-BUTYL-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER

Synonyms:

Suppliers and Price of BETA-OXO-4-TERT-BUTYL-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Total 1 raw suppliers
Chemical Property of BETA-OXO-4-TERT-BUTYL-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER Edit
Chemical Property:
  • Boiling Point:356.2±25.0 °C(Predicted) 
  • PKA:10.17±0.25(Predicted) 
  • Density:1.009±0.06 g/cm3(Predicted) 
Purity/Quality:

95+% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of BETA-OXO-4-TERT-BUTYL-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER

There total 2 articles about BETA-OXO-4-TERT-BUTYL-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER 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:
Guidance literature:
acetic acid tert-butyl ester; With n-butyllithium; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;
N-methoxy-N-methyl-4-(2-methyl-2-propanyl)benzamide; In tetrahydrofuran; hexane; at -78 ℃; for 1h;
DOI:10.1021/acs.orglett.1c02744
Guidance literature:
Multi-step reaction with 2 steps
1.1: triethylamine / dichloromethane / 3 h / 0 - 20 °C
2.1: n-butyllithium; N-ethyl-N,N-diisopropylamine / hexane; tetrahydrofuran / 0.5 h / -78 °C
2.2: 1 h / -78 °C
With n-butyllithium; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1021/acs.orglett.1c02744
Guidance literature:
With C59H69N4O3(1+)*Br(1-); caesium carbonate; In water; toluene; at 20 ℃; Overall yield = 76 percent; Overall yield = 72 mg; enantioselective reaction;
DOI:10.1021/acs.orglett.1c02744
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