(2-benzyl-1,1-dioxo-1λ⁶-[1,2]thiazinan-6-yl)-phosphonic acid diethyl ester

Base Information

Chemical Name:(2-benzyl-1,1-dioxo-1λ⁶-[1,2]thiazinan-6-yl)-phosphonic acid diethyl ester
CAS No.:905975-33-9
Molecular Formula:C₁₅H₂₄NO₅PS
Molecular Weight:361.399
Hs Code.:

(2-benzyl-1,1-dioxo-1λ<sup>6</sup>-[1,2]thiazinan-6-yl)-phosphonic acid diethyl ester

Synonyms:(2-benzyl-1,1-dioxo-1λ⁶-[1,2]thiazinan-6-yl)-phosphonic acid diethyl ester

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Chemical Property of (2-benzyl-1,1-dioxo-1λ⁶-[1,2]thiazinan-6-yl)-phosphonic acid diethyl ester

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Technology Process of (2-benzyl-1,1-dioxo-1λ⁶-[1,2]thiazinan-6-yl)-phosphonic acid diethyl ester

There total 4 articles about (2-benzyl-1,1-dioxo-1λ⁶-[1,2]thiazinan-6-yl)-phosphonic acid diethyl 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:

Reference yield: 34.0%

: 814-49-3
diethyl chlorophosphate

: 37441-51-3
2-benzyl-1,2-thiazinane 1,1-dioxide

: 905975-33-9
(2-benzyl-1,1-dioxo-1λ⁶-[1,2]thiazinan-6-yl)-phosphonic acid diethyl ester

Guidance literature:: 2-benzyl-1,2-thiazinane 1,1-dioxide; With lithium diisopropyl amide; In tetrahydrofuran; hexane; at -78 ℃; for 0.166667h;

diethyl chlorophosphate; In tetrahydrofuran; hexane; at -78 ℃; for 1h;
DOI:10.1016/j.bmcl.2006.04.079

Reference yield:

: 100-46-9
benzylamine

: 905975-33-9
(2-benzyl-1,1-dioxo-1λ⁶-[1,2]thiazinan-6-yl)-phosphonic acid diethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 100 °C

2.1: POCl₃ / Heating

3.1: K₂CO₃ / ethyl acetate / 20 °C

4.1: LDA / hexane; tetrahydrofuran / 0.17 h / -78 °C

4.2: 34 percent / tetrahydrofuran; hexane / 1 h / -78 °C

With potassium carbonate; lithium diisopropyl amide; trichlorophosphate; In tetrahydrofuran; hexane; ethyl acetate; 4.2: Wittig-Horner reaction;
DOI:10.1016/j.bmcl.2006.04.079

Reference yield:

: 4-benzylamino-butane-1-sulfonyl chloride

: 905975-33-9
(2-benzyl-1,1-dioxo-1λ⁶-[1,2]thiazinan-6-yl)-phosphonic acid diethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: K₂CO₃ / ethyl acetate / 20 °C

2.1: LDA / hexane; tetrahydrofuran / 0.17 h / -78 °C

2.2: 34 percent / tetrahydrofuran; hexane / 1 h / -78 °C

With potassium carbonate; lithium diisopropyl amide; In tetrahydrofuran; hexane; ethyl acetate; 2.2: Wittig-Horner reaction;
DOI:10.1016/j.bmcl.2006.04.079