(1S,2R,3S,4R,7S,8R)-3-Benzyloxy-7,8-bis-benzyloxymethyl-4-methyl-2-vinyl-bicyclo[2.2.2]oct-5-en-2-ol

Base Information

Chemical Name:(1S,2R,3S,4R,7S,8R)-3-Benzyloxy-7,8-bis-benzyloxymethyl-4-methyl-2-vinyl-bicyclo[2.2.2]oct-5-en-2-ol
CAS No.:176659-65-7
Molecular Formula:C₃₄H₃₈O₄
Molecular Weight:510.673
Hs Code.:

Synonyms:(1S,2R,3S,4R,7S,8R)-3-Benzyloxy-7,8-bis-benzyloxymethyl-4-methyl-2-vinyl-bicyclo[2.2.2]oct-5-en-2-ol

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Chemical Property of (1S,2R,3S,4R,7S,8R)-3-Benzyloxy-7,8-bis-benzyloxymethyl-4-methyl-2-vinyl-bicyclo[2.2.2]oct-5-en-2-ol

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Technology Process of (1S,2R,3S,4R,7S,8R)-3-Benzyloxy-7,8-bis-benzyloxymethyl-4-methyl-2-vinyl-bicyclo[2.2.2]oct-5-en-2-ol

There total 8 articles about (1S,2R,3S,4R,7S,8R)-3-Benzyloxy-7,8-bis-benzyloxymethyl-4-methyl-2-vinyl-bicyclo[2.2.2]oct-5-en-2-ol 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:

: 100-39-0
benzyl bromide

: 176659-64-6
(1R,2S,3R,4S,7R,8S)-7,8-Bis-benzyloxymethyl-1-methyl-3-vinyl-bicyclo[2.2.2]oct-5-ene-2,3-diol

: 176659-65-7
(1S,2R,3S,4R,7S,8R)-3-Benzyloxy-7,8-bis-benzyloxymethyl-4-methyl-2-vinyl-bicyclo[2.2.2]oct-5-en-2-ol

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 0 - 18 ℃; for 2h; Yield given;
DOI:10.1039/cc9960000869

Reference yield:

: 114763-30-3
(3aR,7aS)-2,2,4-trimethyl-3a,7a-dihydro-1,3-benzodioxole

: 176659-65-7
(1S,2R,3S,4R,7S,8R)-3-Benzyloxy-7,8-bis-benzyloxymethyl-4-methyl-2-vinyl-bicyclo[2.2.2]oct-5-en-2-ol

Guidance literature:: Multi-step reaction with 8 steps

1: 68 percent / CH₂Cl₂ / 24 h / 0 - 18 °C

2: 88 percent / LiAlH₄ / tetrahydrofuran / 3 h / 66 °C

3: 99 percent / NaH, Bu₄NI / dimethylformamide / 18 h / 0 - 18 °C

4: 100 percent / aq. AcOH / 16 h / 80 °C

5: 97 percent / 4-AcNH-TEMPO, p-TsOH / CH₂Cl₂ / 3 h / 18 °C

6: 60 percent / PPh₃, DEAD / 0.5 h / 0 - 18 °C

7: tetrahydrofuran / 3 h / 0 °C

8: NaH / dimethylformamide / 2 h / 0 - 18 °C

With 4-acetylamino-2,2,6,6-tetramethylpiperidine-N-oxyl; lithium aluminium tetrahydride; tetra-(n-butyl)ammonium iodide; sodium hydride; toluene-4-sulfonic acid; acetic acid; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1039/cc9960000869

Reference yield:

: 176659-49-7
((1S,2S,6R,7R,8R,9S)-9-Hydroxymethyl-4,4,7-trimethyl-3,5-dioxa-tricyclo[5.2.2.0^2,6]undec-10-en-8-yl)-methanol

: 176659-65-7
(1S,2R,3S,4R,7S,8R)-3-Benzyloxy-7,8-bis-benzyloxymethyl-4-methyl-2-vinyl-bicyclo[2.2.2]oct-5-en-2-ol

Guidance literature:: Multi-step reaction with 6 steps

1: 99 percent / NaH, Bu₄NI / dimethylformamide / 18 h / 0 - 18 °C

2: 100 percent / aq. AcOH / 16 h / 80 °C

3: 97 percent / 4-AcNH-TEMPO, p-TsOH / CH₂Cl₂ / 3 h / 18 °C

4: 60 percent / PPh₃, DEAD / 0.5 h / 0 - 18 °C

5: tetrahydrofuran / 3 h / 0 °C

6: NaH / dimethylformamide / 2 h / 0 - 18 °C

With 4-acetylamino-2,2,6,6-tetramethylpiperidine-N-oxyl; tetra-(n-butyl)ammonium iodide; sodium hydride; toluene-4-sulfonic acid; acetic acid; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1039/cc9960000869