tert-butylallyl(2-(isothiazol-5-yl)-2-oxoethyl)carbamate

Base Information

Chemical Name:tert-butylallyl(2-(isothiazol-5-yl)-2-oxoethyl)carbamate
CAS No.:1463484-37-8
Molecular Formula:C₁₃H₁₈N₂O₃S
Molecular Weight:282.364
Hs Code.:
Mol file:1463484-37-8.mol

Synonyms:tert-butyl N-allyl-N-(2-isothiazol-5-yl-2-oxo-ethyl)carbamate

Suppliers and Price of tert-butylallyl(2-(isothiazol-5-yl)-2-oxoethyl)carbamate

Supply Marketing:

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

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Total 2 raw suppliers

Chemical Property of tert-butylallyl(2-(isothiazol-5-yl)-2-oxoethyl)carbamate

Chemical Property:

Purity/Quality:: 99% ^*data from raw suppliers

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Technology Process of tert-butylallyl(2-(isothiazol-5-yl)-2-oxoethyl)carbamate

There total 6 articles about tert-butylallyl(2-(isothiazol-5-yl)-2-oxoethyl)carbamate 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: 86.0%

: 288-16-4
isothiazol

: 1429646-79-6
tert-butyl N-allyl-N-[2-(methoxy(methyl)amino)-2-oxo-ethyl]carbamate

: 1463484-37-8
tert-butyl N-allyl-N-(2-isothiazol-5-yl-2-oxo-ethyl)carbamate

Guidance literature:: isothiazol; With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃; for 0.5h;

tert-butyl N-allyl-N-[2-(methoxy(methyl)amino)-2-oxo-ethyl]carbamate; In tetrahydrofuran; at -78 - 20 ℃; for 1.25h; Temperature; Time;

Reference yield:

: 145618-68-4
2-(allyl(tert-butoxycarbonyl)amino)acetic acid

: 1463484-37-8
tert-butyl N-allyl-N-(2-isothiazol-5-yl-2-oxo-ethyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / tetrahydrofuran / 3 h / 0 - 20 °C

1.2: 3 h / 0 - 20 °C

2.1: lithium diisopropyl amide / tetrahydrofuran / 0.5 h / -78 °C

2.2: 1.25 h / -78 - 20 °C

With triethylamine; lithium diisopropyl amide; In tetrahydrofuran;

Reference yield:

: 3182-77-2
N-allylglycine

: 1463484-37-8
tert-butyl N-allyl-N-(2-isothiazol-5-yl-2-oxo-ethyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / ethanol / 0 - 20 °C

1.2: 3 h / 20 °C

2.1: triethylamine / tetrahydrofuran / 3 h / 0 - 20 °C

2.2: 3 h / 0 - 20 °C

3.1: lithium diisopropyl amide / tetrahydrofuran / 0.5 h / -78 °C

3.2: 1.25 h / -78 - 20 °C

With triethylamine; lithium diisopropyl amide; In tetrahydrofuran; ethanol;