(4S,5R)-3-((2R)-2,5-dimethyl-hex-4-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one

Base Information

Chemical Name:(4S,5R)-3-((2R)-2,5-dimethyl-hex-4-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one
CAS No.:312962-11-1
Molecular Formula:C₁₈H₂₃NO₃
Molecular Weight:301.386
Hs Code.:

Synonyms:(4S,5R)-3-((2R)-2,5-dimethyl-hex-4-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one

Suppliers and Price of (4S,5R)-3-((2R)-2,5-dimethyl-hex-4-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one

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 (4S,5R)-3-((2R)-2,5-dimethyl-hex-4-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (4S,5R)-3-((2R)-2,5-dimethyl-hex-4-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one

There total 2 articles about (4S,5R)-3-((2R)-2,5-dimethyl-hex-4-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one 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: 85.0%

: 77877-20-4,116382-72-0,143654-01-7
(4S,5R)-4-methyl-5-phenyl-3-propionyloxazolidin-2-one

: 870-63-3
prenyl bromide

: 312962-11-1
(4S,5R)-3-((2R)-2,5-dimethyl-hex-4-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one

Guidance literature:: (4S,5R)-4-methyl-5-phenyl-3-propionyloxazolidin-2-one; With lithium hexamethyldisilazane; In tetrahydrofuran; at -78 ℃; for 0.5h;

prenyl bromide; In tetrahydrofuran; at 0 ℃; for 16h; Further stages.;
DOI:10.1021/ol006646d

Reference yield:

: 16251-45-9,17097-67-5,28044-22-6,28044-23-7,39663-75-7,54418-69-8,77943-39-6,125133-96-2,149055-02-7
(4S,5R)-4-methyl-5-phenyl-oxazolidin-2-one

: 312962-11-1
(4S,5R)-3-((2R)-2,5-dimethyl-hex-4-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / -78 °C

1.2: -78 - 20 °C

2.1: sodium hexamethyldisilazane / tetrahydrofuran / -78 °C

2.2: 18 h / -78 °C

With n-butyllithium; sodium hexamethyldisilazane; In tetrahydrofuran; hexane;
DOI:10.1016/j.tet.2021.132118

Reference yield:

: 312962-11-1
(4S,5R)-3-((2R)-2,5-dimethyl-hex-4-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one

: 312962-24-6
2-allyl-6-methoxymethoxy-benzoic acid (1R,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4,7-dimethyl-oct-6-enyl ester

Guidance literature:: Multi-step reaction with 11 steps

1.1: 99 percent / LiOH*H₂O; H₂O₂ / tetrahydrofuran / 4 h / 0 °C

2.1: (1-chloro-2-methyl-propenyl)-dimethyl-amine / CH₂Cl₂ / 1.5 h

3.1: diisopropylamine; n-BuLi / tetrahydrofuran; hexane / 1 h / -78 °C

3.2: 3.50 g / tetrahydrofuran; hexane / 2 h / 20 °C

4.1: 96 percent / H₂ / [(R)-BINAP*RuCl₂]2*NEt₃ / methanol / 4 h / 80 °C / 3040.2 Torr

5.1: 90 percent / diisopropylethylamine; N,N-dimethylaminopyridine / CH₂Cl₂ / 40 h / 20 °C

6.1: LiHMDS / tetrahydrofuran / 1.5 h / -45 - -30 °C

6.2: 98 percent / tetrahydrofuran / 3 h / -40 - -30 °C

7.1: 93 percent / H₂ / [(R)-BINAP*RuCl₂]*NEt₃ / methanol / 6.5 h / 25 °C / 60804.1 Torr

8.1: 98 percent / LiAlH₄ / diethyl ether / 6 h / 0 °C

9.1: NaH / dimethylformamide / 1.25 h

9.2: 85 percent / dimethylformamide / 1.5 h

10.1: 88 percent / DEAD; PPh₃ / diethyl ether / 20 h / 20 °C

11.1: 84 percent / diisopropylethylamine / CH₂Cl₂ / 18 h

With dmap; lithium hydroxide; lithium aluminium tetrahydride; n-butyllithium; 1-chloro-1-(dimethylamino)-2-methyl-1-propene; hydrogen; dihydrogen peroxide; sodium hydride; diisopropylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; lithium hexamethyldisilazane; diethylazodicarboxylate; [(R)-BINAP RuCl₂]2NEt₃; [(R)-BINAP*RuCl₂]*NEt₃; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; N,N-dimethyl-formamide; 1.1: Hydrolysis / 2.1: Substitution / 3.1: deprotonation / 3.2: Substitution / 4.1: Catalytic hydrogenation / 5.1: Alkylation / 6.1: Metallation / 6.2: Metallation / 7.1: Catalytic hydrogenation / 8.1: Reduction / 9.1: deprotonation / 9.2: Alkylation / 10.1: Esterification / 11.1: Alkylation;
DOI:10.1021/ol006646d