(R)-2-Benzyloxy-2-((3aS,6S,6aS)-1-methyl-hexahydro-pyrrolo[3,4-c]isoxazol-6-yl)-ethanol

Base Information

Chemical Name:(R)-2-Benzyloxy-2-((3aS,6S,6aS)-1-methyl-hexahydro-pyrrolo[3,4-c]isoxazol-6-yl)-ethanol
CAS No.:423158-03-6
Molecular Formula:C₁₅H₂₂N₂O₃
Molecular Weight:278.351
Hs Code.:

Synonyms:(R)-2-Benzyloxy-2-((3aS,6S,6aS)-1-methyl-hexahydro-pyrrolo[3,4-c]isoxazol-6-yl)-ethanol

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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 (R)-2-Benzyloxy-2-((3aS,6S,6aS)-1-methyl-hexahydro-pyrrolo[3,4-c]isoxazol-6-yl)-ethanol

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Technology Process of (R)-2-Benzyloxy-2-((3aS,6S,6aS)-1-methyl-hexahydro-pyrrolo[3,4-c]isoxazol-6-yl)-ethanol

There total 2 articles about (R)-2-Benzyloxy-2-((3aS,6S,6aS)-1-methyl-hexahydro-pyrrolo[3,4-c]isoxazol-6-yl)-ethanol 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%

: 423158-00-3
(R)-Benzyloxy-((3aS,6S,6aS)-1-methyl-hexahydro-pyrrolo[3,4-c]isoxazol-6-yl)-acetic acid methyl ester

: 423158-03-6
(R)-2-Benzyloxy-2-((3aS,6S,6aS)-1-methyl-hexahydro-pyrrolo[3,4-c]isoxazol-6-yl)-ethanol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; at 20 ℃;
DOI:10.1055/s-2002-19333

Reference yield:

: 253599-41-6
(+)-(3R,4R)-3-benzyloxy-1-(2-propenyl)-4-oxoazetidine-2-carbaldehyde

: 423158-03-6
(R)-2-Benzyloxy-2-((3aS,6S,6aS)-1-methyl-hexahydro-pyrrolo[3,4-c]isoxazol-6-yl)-ethanol

Guidance literature:: Multi-step reaction with 2 steps

1: 50 percent / Na₂CO₃ / Heating

2: 100 percent / LiAlH₄ / diethyl ether / 20 °C

With lithium aluminium tetrahydride; sodium carbonate; In diethyl ether;
DOI:10.1055/s-2002-19333