(3S,6R,7aR)-5-oxo-3-phenylhexahydropyrrolo[1,2-c]oxazol-6-yl-methanesulfonate

Base Information

Chemical Name:(3S,6R,7aR)-5-oxo-3-phenylhexahydropyrrolo[1,2-c]oxazol-6-yl-methanesulfonate
CAS No.:1613043-71-2
Molecular Formula:C₁₃H₁₅NO₅S
Molecular Weight:297.332
Hs Code.:

Synonyms:(3S,6R,7aR)-5-oxo-3-phenylhexahydropyrrolo[1,2-c]oxazol-6-yl-methanesulfonate

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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 (3S,6R,7aR)-5-oxo-3-phenylhexahydropyrrolo[1,2-c]oxazol-6-yl-methanesulfonate

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Technology Process of (3S,6R,7aR)-5-oxo-3-phenylhexahydropyrrolo[1,2-c]oxazol-6-yl-methanesulfonate

There total 6 articles about (3S,6R,7aR)-5-oxo-3-phenylhexahydropyrrolo[1,2-c]oxazol-6-yl-methanesulfonate 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%

: 1311406-94-6
(3S,6R,7aR)-6-hydroxy-3-phenyltetrahydropyrrolo[1,2-c]oxazol-5(3H)-one

: 124-63-0
methanesulfonyl chloride

: 1613043-71-2
(3S,6R,7aR)-5-oxo-3-phenylhexahydropyrrolo[1,2-c]oxazol-6-yl-methanesulfonate

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 20h;
DOI:10.1002/ejoc.201301773

Reference yield:

: 6893-26-1,21675-62-7,23009-64-5,25104-13-6,84960-48-5,25513-46-6
D-Glutamic acid

: 1613043-71-2
(3S,6R,7aR)-5-oxo-3-phenylhexahydropyrrolo[1,2-c]oxazol-6-yl-methanesulfonate

Guidance literature:: Multi-step reaction with 5 steps

1.1: thionyl chloride / 20 h / 20 °C

1.2: 2 h / Reflux

2.1: sodium tetrahydroborate / isopropyl alcohol / 20 h / 20 °C

3.1: toluene-4-sulfonic acid; water / toluene / 20 °C / Reflux

4.1: diisopropylamine; n-butyllithium / tetrahydrofuran; hexane / 0.83 h / -78 °C

4.2: -78 - -35 °C

5.1: triethylamine / dichloromethane / 20 h / 0 - 20 °C

With sodium tetrahydroborate; n-butyllithium; thionyl chloride; water; toluene-4-sulfonic acid; triethylamine; diisopropylamine; In tetrahydrofuran; hexane; dichloromethane; isopropyl alcohol; toluene;
DOI:10.1002/ejoc.201301773

Reference yield:

: 118918-76-6,1820583-17-2
(2S,5R)-2-phenyl-1-aza-3-oxabicyclo<3.3.0>octan-8-one

: 1613043-71-2
(3S,6R,7aR)-5-oxo-3-phenylhexahydropyrrolo[1,2-c]oxazol-6-yl-methanesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1.1: diisopropylamine; n-butyllithium / tetrahydrofuran; hexane / 0.83 h / -78 °C

1.2: -78 - -35 °C

2.1: triethylamine / dichloromethane / 20 h / 0 - 20 °C

With n-butyllithium; triethylamine; diisopropylamine; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1002/ejoc.201301773