(-)-(S)-S-1-Methyl-1-phenylpropyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-thiocarboxylate

Base Information

Chemical Name:(-)-(S)-S-1-Methyl-1-phenylpropyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-thiocarboxylate
CAS No.:334757-32-3
Molecular Formula:C₁₈H₂₇NO₂S
Molecular Weight:321.484
Hs Code.:

Synonyms:(-)-(S)-S-1-Methyl-1-phenylpropyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-thiocarboxylate

Suppliers and Price of (-)-(S)-S-1-Methyl-1-phenylpropyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-thiocarboxylate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (-)-(S)-S-1-Methyl-1-phenylpropyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-thiocarboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (-)-(S)-S-1-Methyl-1-phenylpropyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-thiocarboxylate

There total 4 articles about (-)-(S)-S-1-Methyl-1-phenylpropyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-thiocarboxylate 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: 90.0%

: 75-03-6
ethyl iodide

: 334757-17-4
(-)-(S)-S-Phenylethyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-thiocarboxylate

: 334757-32-3
(-)-(S)-S-1-Methyl-1-phenylpropyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-thiocarboxylate

Guidance literature:: (-)-(S)-S-Phenylethyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-thiocarboxylate; With N,N,N,N,-tetramethylethylenediamine; sec.-butyllithium; In diethyl ether; cyclohexane; at -78 ℃; for 2h;

ethyl iodide; In diethyl ether; cyclohexane; at -78 ℃; Further stages.;
DOI:10.1002/1521-3765(20010119)7:2<423::AID-CHEM423>3.0.CO;2-Y

Reference yield:

: 33877-11-1
(S)-1-mercapto-1-phenylethane

: 334757-32-3
(-)-(S)-S-1-Methyl-1-phenylpropyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-thiocarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: NaH / tetrahydrofuran / 0.5 h / 20 °C

1.2: 97 percent / tetrahydrofuran / 3 h / Heating

2.1: TMEDA; sec-BuLi / diethyl ether; cyclohexane / 2 h / -78 °C

2.2: 90 percent / diethyl ether; cyclohexane / -78 °C

With N,N,N,N,-tetramethylethylenediamine; sec.-butyllithium; sodium hydride; In tetrahydrofuran; diethyl ether; cyclohexane;
DOI:10.1002/1521-3765(20010119)7:2<423::AID-CHEM423>3.0.CO;2-Y

Reference yield:

: 62258-06-4,67385-07-3,133098-85-8
thioacetic acid S-((S)-1-phenylethyl) ester

: 334757-32-3
(-)-(S)-S-1-Methyl-1-phenylpropyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-thiocarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: 3.75 g / LiAlH₄ / diethyl ether / 2 h / Heating

2.1: NaH / tetrahydrofuran / 0.5 h / 20 °C

2.2: 97 percent / tetrahydrofuran / 3 h / Heating

3.1: TMEDA; sec-BuLi / diethyl ether; cyclohexane / 2 h / -78 °C

3.2: 90 percent / diethyl ether; cyclohexane / -78 °C

With lithium aluminium tetrahydride; N,N,N,N,-tetramethylethylenediamine; sec.-butyllithium; sodium hydride; In tetrahydrofuran; diethyl ether; cyclohexane;
DOI:10.1002/1521-3765(20010119)7:2<423::AID-CHEM423>3.0.CO;2-Y