(4S,6R)-4-Allyl-6-((R)-2-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-one

Base Information

Chemical Name:(4S,6R)-4-Allyl-6-((R)-2-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-one
CAS No.:909257-43-8
Molecular Formula:C₁₈H₂₄O₃
Molecular Weight:288.387
Hs Code.:

Synonyms:(4S,6R)-4-Allyl-6-((R)-2-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-one

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Chemical Property of (4S,6R)-4-Allyl-6-((R)-2-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-one

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Technology Process of (4S,6R)-4-Allyl-6-((R)-2-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-one

There total 5 articles about (4S,6R)-4-Allyl-6-((R)-2-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-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: 90.0%

: 909257-40-5
(R)-6-((R)-2-Benzyloxy-1-methyl-ethyl)-5,6-dihydro-pyran-2-one

: 21500-57-2,33462-38-3,33462-39-4,53450-34-3,94901-46-9
lithium dilallyl cuprate

: 909257-43-8
(4S,6R)-4-Allyl-6-((R)-2-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-one

Guidance literature:: In tetrahydrofuran; at -78 - -40 ℃;
DOI:10.1016/j.tetlet.2006.06.046

Reference yield:

: 79026-61-2
(R)-3-benzyloxy-2-methylpropanal

: 909257-43-8
(4S,6R)-4-Allyl-6-((R)-2-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: 93 percent / SnCl₄ / CH₂Cl₂ / -90 °C

2.1: 1,4-nitrobenzoic acid; PPh₃; DEAD / tetrahydrofuran

2.2: NaOH / methanol

3.1: 80 percent / Et₃N / CH₂Cl₂

4.1: 80 percent / Grubbs' catalyst / CH₂Cl₂ / 24 h

5.1: 90 percent / tetrahydrofuran / -78 - -40 °C

With tin(IV) chloride; triethylamine; triphenylphosphine; diethylazodicarboxylate; 4-nitro-benzoic acid; Grubbs catalyst first generation; In tetrahydrofuran; dichloromethane; 1.1: Mitsunobu reaction / 5.1: Michael reaction;
DOI:10.1016/j.tetlet.2006.06.046

Reference yield:

: 94233-73-5
(2R,3R)-1-(benzyloxy)-2-methylhex-5-en-3-ol

: 909257-43-8
(4S,6R)-4-Allyl-6-((R)-2-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / Et₃N / CH₂Cl₂

2: 80 percent / Grubbs' catalyst / CH₂Cl₂ / 24 h

3: 90 percent / tetrahydrofuran / -78 - -40 °C

With triethylamine; Grubbs catalyst first generation; In tetrahydrofuran; dichloromethane; 3: Michael reaction;
DOI:10.1016/j.tetlet.2006.06.046