(3aR,5R,6R,6aR)-2,2-Dimethyl-5-(2-trityloxy-ethyl)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

Base Information

Chemical Name:(3aR,5R,6R,6aR)-2,2-Dimethyl-5-(2-trityloxy-ethyl)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol
CAS No.:479668-95-6
Molecular Formula:C₃₀H₃₂O₅
Molecular Weight:472.581
Hs Code.:

Synonyms:(3aR,5R,6R,6aR)-2,2-Dimethyl-5-(2-trityloxy-ethyl)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

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Chemical Property of (3aR,5R,6R,6aR)-2,2-Dimethyl-5-(2-trityloxy-ethyl)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

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Technology Process of (3aR,5R,6R,6aR)-2,2-Dimethyl-5-(2-trityloxy-ethyl)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

There total 2 articles about (3aR,5R,6R,6aR)-2,2-Dimethyl-5-(2-trityloxy-ethyl)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-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: 75.0%

: Imidazole-1-carbothioic acid O-[(R)-1-((3aR,5R,6R,6aR)-6-hydroxy-2,2-dimethyl-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-2-trityloxy-ethyl] ester

: 479668-95-6
(3aR,5R,6R,6aR)-2,2-Dimethyl-5-(2-trityloxy-ethyl)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

Guidance literature:: With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In toluene; Heating;
DOI:10.1016/S0040-4039(02)02058-0

Reference yield:

: 322390-88-5
1,2-O-Isopropylidene-6-O-triphenylmethyl-3-C-vinyl-α-D-allofuranose

: 479668-95-6
(3aR,5R,6R,6aR)-2,2-Dimethyl-5-(2-trityloxy-ethyl)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / DMAP / CH₂Cl₂ / 20 °C

2: 75 percent / Bu₃SnH; AIBN / toluene / Heating

With dmap; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In dichloromethane; toluene;
DOI:10.1016/S0040-4039(02)02058-0

Reference yield:

: 479668-95-6
(3aR,5R,6R,6aR)-2,2-Dimethyl-5-(2-trityloxy-ethyl)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

: (2S,3R,3aS,4S,5R,6S,7aR)-3a,6-Bis-benzyloxy-4,5-bis-benzyloxymethyl-5-methyl-octahydro-benzofuran-2,3-diol

Guidance literature:: Multi-step reaction with 10 steps

1: 78 percent / Na / liquid ammonia; tetrahydrofuran / -78 °C

2: Dess-Martin periodinane / CH₂Cl₂ / 20 °C

3: tetrahydrofuran / 0 °C

4: 100 percent / Et₃N / CH₂Cl₂ / 20 °C

5: 58 percent / benzoyl peroxide / 3 h / Heating

6: 72 percent / dimethylsulfoxide / 120 °C

7: 65 percent / O₃; NaHCO₃; Me₂S / CH₂Cl₂ / -78 - 20 °C

8: 100 percent / LiAlH₄ / tetrahydrofuran / 0 - 50 °C

9: 100 percent / Bu₄NI / dimethylformamide / 0 - 60 °C

10: aq. HCl / acetic acid; tetrahydrofuran / Heating

With hydrogenchloride; lithium aluminium tetrahydride; dimethylsulfide; sodium; tetra-(n-butyl)ammonium iodide; sodium hydrogencarbonate; Dess-Martin periodane; ozone; triethylamine; dibenzoyl peroxide; In tetrahydrofuran; dichloromethane; ammonia; acetic acid; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(02)02058-0