(R)-(3-ethyl-2-oxopiperidin-3-yl)methyl 4-methylbenzenesulfonate

Base Information

Chemical Name:(R)-(3-ethyl-2-oxopiperidin-3-yl)methyl 4-methylbenzenesulfonate
CAS No.:1320327-58-9
Molecular Formula:C₁₅H₂₁NO₄S
Molecular Weight:311.402
Hs Code.:

Synonyms:(R)-(3-ethyl-2-oxopiperidin-3-yl)methyl 4-methylbenzenesulfonate

Suppliers and Price of (R)-(3-ethyl-2-oxopiperidin-3-yl)methyl 4-methylbenzenesulfonate

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 (R)-(3-ethyl-2-oxopiperidin-3-yl)methyl 4-methylbenzenesulfonate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-(3-ethyl-2-oxopiperidin-3-yl)methyl 4-methylbenzenesulfonate

There total 12 articles about (R)-(3-ethyl-2-oxopiperidin-3-yl)methyl 4-methylbenzenesulfonate 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: 84.0%

: 1320327-55-6
(R)-3-ethyl-3-(hydroxymethyl)piperidin-2-one

: 98-59-9
p-toluenesulfonyl chloride

: 1320327-58-9
(R)-(3-ethyl-2-oxopiperidin-3-yl)methyl 4-methylbenzenesulfonate

Guidance literature:: With pyridine; at 20 ℃; Cooling with ice;
DOI:10.1021/ol201892j

Reference yield:

: 1320327-43-2
(4aS,9aS)-4a-allyl-4a,7,8,9,9a,10-hexahydropyrido [3,2-f] pyrrolo [2, 1-c][1,4]oxazepin-5(2H)-one

: 1320327-58-9
(R)-(3-ethyl-2-oxopiperidin-3-yl)methyl 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 6 steps

1: sulfuric acid / methanol / 75 h / 20 °C

2: 2,6-dimethylpyridine; sodium periodate; osmium(VIII) oxide / 1,4-dioxane; water; tert-butyl alcohol / 4 h / 25 °C

3: boron trifluoride diethyl etherate / dichloromethane / 12 h / Reflux

4: hydrogen / ethanol / 7 h / 760.05 Torr / Reflux

5: sodium tetrahydroborate; cerium(III) chloride heptahydrate / ethanol / 48 h / 20 °C

6: pyridine / 20 °C / Cooling with ice

With pyridine; 2,6-dimethylpyridine; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; cerium(III) chloride heptahydrate; sulfuric acid; boron trifluoride diethyl etherate; hydrogen; In 1,4-dioxane; methanol; ethanol; dichloromethane; water; tert-butyl alcohol;
DOI:10.1021/ol201892j

Reference yield:

: 100044-96-0
1,2,3,10,11,11a(S)-hexahydro-5H-pyrrolo<2,1-c>pyrido<3,2-f><1,4>oxazepin-5-one

: 1320327-58-9
(R)-(3-ethyl-2-oxopiperidin-3-yl)methyl 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 8 steps

1: ammonia; sodium; tert-butyl alcohol / tetrahydrofuran / 0.83 h / -78 °C

2: isoprene / tetrahydrofuran / 3 h / -78 °C

3: sulfuric acid / methanol / 75 h / 20 °C

4: 2,6-dimethylpyridine; sodium periodate; osmium(VIII) oxide / 1,4-dioxane; water; tert-butyl alcohol / 4 h / 25 °C

5: boron trifluoride diethyl etherate / dichloromethane / 12 h / Reflux

6: hydrogen / ethanol / 7 h / 760.05 Torr / Reflux

7: sodium tetrahydroborate; cerium(III) chloride heptahydrate / ethanol / 48 h / 20 °C

8: pyridine / 20 °C / Cooling with ice

With pyridine; 2,6-dimethylpyridine; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; cerium(III) chloride heptahydrate; sulfuric acid; boron trifluoride diethyl etherate; ammonia; hydrogen; sodium; tert-butyl alcohol; isoprene; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; water; tert-butyl alcohol; 1: Birch reduction;
DOI:10.1021/ol201892j