(S)-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-methoxy-acetaldehyde

Base Information

Chemical Name:(S)-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-methoxy-acetaldehyde
CAS No.:119841-62-2
Molecular Formula:C₃₀H₃₆O₅Si
Molecular Weight:504.698
Hs Code.:

Synonyms:(S)-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-methoxy-acetaldehyde

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Chemical Property of (S)-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-methoxy-acetaldehyde

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Technology Process of (S)-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-methoxy-acetaldehyde

There total 9 articles about (S)-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-methoxy-acetaldehyde 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:

: (R)-2-[(2R,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-2-methoxy-ethanol

: 119841-62-2
(S)-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-methoxy-acetaldehyde

Guidance literature:: With pyridinium chlorochromate absorbed on neutral alumina; at -60 ℃; Yield given;
DOI:10.1016/0040-4039(88)85177-3

Reference yield:

: 100-39-0
benzyl bromide

: 119841-62-2
(S)-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-methoxy-acetaldehyde

Guidance literature:: Multi-step reaction with 6 steps

1: NaH / tetrahydrofuran / 0 - 22 °C

2: p-TsOH / methanol / 14 h / 22 °C

3: Et₃N, DMAP / CH₂Cl₂ / -78 - -40 °C

4: NaH / dimethylformamide / 0 °C

5: LiOH, H₂O / tetrahydrofuran

6: PCC-Al₂O₃ / -60 °C

With dmap; lithium hydroxide; pyridinium chlorochromate absorbed on neutral alumina; water; sodium hydride; toluene-4-sulfonic acid; triethylamine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/0040-4039(88)85177-3

Reference yield:

: (2S,3R,4S)-2-((S)-4,4-Dimethyl-[1,3]dioxolan-2-yl)-tetrahydro-furan-3,4-diol

: 119841-62-2
(S)-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-methoxy-acetaldehyde

Guidance literature:: Multi-step reaction with 7 steps

1: Et₃N, DMAP / CH₂Cl₂ / -10 - 22 °C

2: NaH / tetrahydrofuran / 0 - 22 °C

3: p-TsOH / methanol / 14 h / 22 °C

4: Et₃N, DMAP / CH₂Cl₂ / -78 - -40 °C

5: NaH / dimethylformamide / 0 °C

6: LiOH, H₂O / tetrahydrofuran

7: PCC-Al₂O₃ / -60 °C

With dmap; lithium hydroxide; pyridinium chlorochromate absorbed on neutral alumina; water; sodium hydride; toluene-4-sulfonic acid; triethylamine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/0040-4039(88)85177-3