tert-butyl (2-{4-[(2,4-dioxo-1,3-thiazolidin-5-yl)methyl]phenoxy}ethyl)methylcarbamate

Base Information

Chemical Name:tert-butyl (2-{4-[(2,4-dioxo-1,3-thiazolidin-5-yl)methyl]phenoxy}ethyl)methylcarbamate
CAS No.:198990-14-6
Molecular Formula:C₁₈H₂₄N₂O₅S
Molecular Weight:380.465
Hs Code.:

Synonyms:tert-butyl (2-{4-[(2,4-dioxo-1,3-thiazolidin-5-yl)methyl]phenoxy}ethyl)methylcarbamate

Suppliers and Price of tert-butyl (2-{4-[(2,4-dioxo-1,3-thiazolidin-5-yl)methyl]phenoxy}ethyl)methylcarbamate

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

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Chemical Property of tert-butyl (2-{4-[(2,4-dioxo-1,3-thiazolidin-5-yl)methyl]phenoxy}ethyl)methylcarbamate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of tert-butyl (2-{4-[(2,4-dioxo-1,3-thiazolidin-5-yl)methyl]phenoxy}ethyl)methylcarbamate

There total 4 articles about tert-butyl (2-{4-[(2,4-dioxo-1,3-thiazolidin-5-yl)methyl]phenoxy}ethyl)methylcarbamate 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: 80.0%

: 905990-90-1
tert-butyl (2-{4-[(Z)-(2,4-dioxo-1,3-thiazolidin-5-ylidene)methyl]phenoxy}ethyl)methylcarbamate

: 198990-14-6
tert-butyl (2-{4-[(2,4-dioxo-1,3-thiazolidin-5-yl)methyl]phenoxy}ethyl)methylcarbamate

Guidance literature:: With magnesium; In ethanol;
DOI:10.1016/S0960-894X(97)10017-8

Reference yield:

: 198990-10-2
tert-butyl (2-(4-formylphenoxy)ethyl)(methyl)carbamate

: 198990-14-6
tert-butyl (2-{4-[(2,4-dioxo-1,3-thiazolidin-5-yl)methyl]phenoxy}ethyl)methylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / benzoic acid; piperidine / toluene / 6 h / Heating

2: 78 percent / Mg; methanol / 4 h / 20 °C

With piperidine; methanol; magnesium; benzoic acid; In toluene;
DOI:10.1021/jm0510880

Reference yield:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 198990-14-6
tert-butyl (2-{4-[(2,4-dioxo-1,3-thiazolidin-5-yl)methyl]phenoxy}ethyl)methylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1: 58 percent / PPh₃; diisopropyl azodicarboxylate / tetrahydrofuran / 3 h / 20 °C

2: 89 percent / benzoic acid; piperidine / toluene / 6 h / Heating

3: 78 percent / Mg; methanol / 4 h / 20 °C

With piperidine; methanol; di-isopropyl azodicarboxylate; magnesium; triphenylphosphine; benzoic acid; In tetrahydrofuran; toluene; 1: Mitsunobu reaction;
DOI:10.1021/jm0510880