(2S,3aS,4S,5R,6S)-6-methyl-2-phenoxyhexahydropyrrolo[1,2-b]isoxazole-4,5-diol

Base Information

Chemical Name:(2S,3aS,4S,5R,6S)-6-methyl-2-phenoxyhexahydropyrrolo[1,2-b]isoxazole-4,5-diol
CAS No.:1314088-79-3
Molecular Formula:C₁₃H₁₇NO₄
Molecular Weight:251.282
Hs Code.:

Synonyms:(2S,3aS,4S,5R,6S)-6-methyl-2-phenoxyhexahydropyrrolo[1,2-b]isoxazole-4,5-diol

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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 (2S,3aS,4S,5R,6S)-6-methyl-2-phenoxyhexahydropyrrolo[1,2-b]isoxazole-4,5-diol

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Technology Process of (2S,3aS,4S,5R,6S)-6-methyl-2-phenoxyhexahydropyrrolo[1,2-b]isoxazole-4,5-diol

There total 7 articles about (2S,3aS,4S,5R,6S)-6-methyl-2-phenoxyhexahydropyrrolo[1,2-b]isoxazole-4,5-diol 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: 100.0%

: 740805-29-2
(2S,3aS,4S,5R,6S)-4,5-isopropylidenedioxy-6-methyl-2-phenoxyhexahydropyrrolo[1,2-b]isoxazole

: 1314088-79-3
(2S,3aS,4S,5R,6S)-6-methyl-2-phenoxyhexahydropyrrolo[1,2-b]isoxazole-4,5-diol

Guidance literature:: With hydrogenchloride; water; In methanol; at 20 ℃; for 16h;
DOI:10.1016/j.carres.2011.03.030

Reference yield:

: 5-deoxy-2,3-O-isopropylidene-4-O-methanesulfonyl-D-ribose O-(tert-butyl-dimethyl)silyl oxime

: 1314088-79-3
(2S,3aS,4S,5R,6S)-6-methyl-2-phenoxyhexahydropyrrolo[1,2-b]isoxazole-4,5-diol

Guidance literature:: Multi-step reaction with 3 steps

1: tetrabutyl ammonium fluoride; triethylamine / acetonitrile / 6 h / 80 °C

2: 1,1,2,2-tetrachloroethane / 16 h / 50 °C

3: hydrogenchloride; water / methanol / 16 h / 20 °C

With hydrogenchloride; tetrabutyl ammonium fluoride; water; triethylamine; In methanol; acetonitrile; 1,1,2,2-tetrachloroethane;
DOI:10.1016/j.carres.2011.03.030

Reference yield:

: 1314088-68-0
5-deoxy-2,3-O-isopropylidene-1,4-di-O-methanesulfonyl-D-ribitol

: 1314088-79-3
(2S,3aS,4S,5R,6S)-6-methyl-2-phenoxyhexahydropyrrolo[1,2-b]isoxazole-4,5-diol

Guidance literature:: Multi-step reaction with 4 steps

1: hydroxylamine hydrochloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine / 85 °C

2: mercury(II) oxide / 6 h / 20 °C

3: 1,1,2,2-tetrachloroethane / 16 h / 50 °C

4: hydrogenchloride; water / methanol / 16 h / 20 °C

With hydrogenchloride; hydroxylamine hydrochloride; water; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; mercury(II) oxide; In methanol; 1,1,2,2-tetrachloroethane;
DOI:10.1016/j.carres.2011.03.030