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tert-butyl 3-(3-fluoropyridin-2-yl)-3-oxopropanoate

Base Information
  • Chemical Name:tert-butyl 3-(3-fluoropyridin-2-yl)-3-oxopropanoate
  • CAS No.:1338091-30-7
  • Molecular Formula:C12H14FNO3
  • Molecular Weight:239.246
  • Hs Code.:
tert-butyl 3-(3-fluoropyridin-2-yl)-3-oxopropanoate

Synonyms:

Suppliers and Price of tert-butyl 3-(3-fluoropyridin-2-yl)-3-oxopropanoate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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  • Crysdot
  • tert-Butyl3-(3-fluoropyridin-2-yl)-3-oxopropanoate 97%
  • 1g
  • $ 842.00
Total 1 raw suppliers
Chemical Property of tert-butyl 3-(3-fluoropyridin-2-yl)-3-oxopropanoate
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

tert-Butyl3-(3-fluoropyridin-2-yl)-3-oxopropanoate 97% *data from reagent suppliers

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Technology Process of tert-butyl 3-(3-fluoropyridin-2-yl)-3-oxopropanoate

There total 2 articles about tert-butyl 3-(3-fluoropyridin-2-yl)-3-oxopropanoate 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 lithium diisopropyl amide; In tetrahydrofuran; n-heptane; at -78 ℃; for 0.75h;
methyl 3-fluoropyridine-2-carboxylate; In tetrahydrofuran; n-heptane; at -78 ℃; for 2h;
Guidance literature:
Multi-step reaction with 2 steps
1.1: sulfuric acid / 20 h / Reflux
2.1: lithium diisopropyl amide / n-heptane; tetrahydrofuran / 0.75 h / -78 °C
2.2: 2 h / -78 °C
With sulfuric acid; lithium diisopropyl amide; In tetrahydrofuran; n-heptane;
Guidance literature:
Multi-step reaction with 6 steps
1.1: triethylamine; 4-acetamidobenzenesulfonyl azide / acetonitrile / 0 - 20 °C
2.1: trimethylphosphane / tetrahydrofuran / 20 °C
2.2: 0.25 h / 20 °C
3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 18 h / 20 °C
4.1: trifluoroacetic acid / dichloromethane / 16 h / 20 °C
5.1: triethylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / dimethyl sulfoxide / 16 h / 20 °C
6.1: hydroxylamine hydrochloride; titanium(IV) isopropylate / toluene / 72 h / Reflux
With titanium(IV) isopropylate; 4-acetamidobenzenesulfonyl azide; hydroxylamine hydrochloride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; trifluoroacetic acid; trimethylphosphane; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; toluene; acetonitrile;
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