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4-[2-(2-tert-Butoxycarbonyl-acetyl)-3-methoxy-phenyl]-3-oxo-butyric acid tert-butyl ester

Base Information Edit
  • Chemical Name:4-[2-(2-tert-Butoxycarbonyl-acetyl)-3-methoxy-phenyl]-3-oxo-butyric acid tert-butyl ester
  • CAS No.:99392-84-4
  • Molecular Formula:C22H30O7
  • Molecular Weight:406.476
  • Hs Code.:
  • Mol file:99392-84-4.mol
4-[2-(2-tert-Butoxycarbonyl-acetyl)-3-methoxy-phenyl]-3-oxo-butyric acid tert-butyl ester

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 4-[2-(2-tert-Butoxycarbonyl-acetyl)-3-methoxy-phenyl]-3-oxo-butyric acid tert-butyl ester Edit
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Technology Process of 4-[2-(2-tert-Butoxycarbonyl-acetyl)-3-methoxy-phenyl]-3-oxo-butyric acid tert-butyl ester

There total 3 articles about 4-[2-(2-tert-Butoxycarbonyl-acetyl)-3-methoxy-phenyl]-3-oxo-butyric acid tert-butyl 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:
Multi-step reaction with 3 steps
1: 2.32 g / potassium carbonate / acetone / 3 h / Heating
2: 2.30 g / conc. sulphuric acid / 3 h / Heating
3: 1) LDA / 1) hexane, -78 deg C, 2) room temp., 20 h
With sulfuric acid; potassium carbonate; lithium diisopropyl amide; In acetone;
Guidance literature:
Multi-step reaction with 2 steps
1: 2.30 g / conc. sulphuric acid / 3 h / Heating
2: 1) LDA / 1) hexane, -78 deg C, 2) room temp., 20 h
With sulfuric acid; lithium diisopropyl amide;
Guidance literature:
With lithium diisopropyl amide; Multistep reaction; 1) hexane, -78 deg C, 2) room temp., 20 h;
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