Benzoic acid, 2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-6-[[(2S,4R,6S)-tetrahydro-6-[(2S )-2-hydroxy-4-pentenyl]-4-(phenylmethoxy)-2H-pyran-2-yl]methyl]-, methyl ester

Base Information

Chemical Name:Benzoic acid, 2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-6-[[(2S,4R,6S)-tetrahydro-6-[(2S )-2-hydroxy-4-pentenyl]-4-(phenylmethoxy)-2H-pyran-2-yl]methyl]-, methyl ester
CAS No.:674336-05-1
Molecular Formula:C42H50O6Si
Molecular Weight:678.941
Hs Code.:

Benzoic acid,
2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-6-[[(2S,4R,6S)-tetrahydro-6-[(2S
)-2-hydroxy-4-pentenyl]-4-(phenylmethoxy)-2H-pyran-2-yl]methyl]-,
methyl ester

Synonyms:

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Chemical Property of Benzoic acid, 2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-6-[[(2S,4R,6S)-tetrahydro-6-[(2S )-2-hydroxy-4-pentenyl]-4-(phenylmethoxy)-2H-pyran-2-yl]methyl]-, methyl ester

Chemical Property:

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Technology Process of Benzoic acid, 2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-6-[[(2S,4R,6S)-tetrahydro-6-[(2S )-2-hydroxy-4-pentenyl]-4-(phenylmethoxy)-2H-pyran-2-yl]methyl]-, methyl ester

There total 11 articles about Benzoic acid, 2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-6-[[(2S,4R,6S)-tetrahydro-6-[(2S )-2-hydroxy-4-pentenyl]-4-(phenylmethoxy)-2H-pyran-2-yl]methyl]-, methyl ester 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%

: 85116-38-7
(+)-diisopinocampheylallylborane

: 674335-94-5
2-[(2S,4R,6R)-4-Benzyloxy-6-(2-oxo-ethyl)-tetrahydro-pyran-2-ylmethyl]-6-(tert-butyl-diphenyl-silanyloxy)-benzoic acid methyl ester

: 674336-05-1
2-[(2S,4R,6S)-4-Benzyloxy-6-((S)-2-hydroxy-pent-4-enyl)-tetrahydro-pyran-2-ylmethyl]-6-(tert-butyl-diphenyl-silanyloxy)-benzoic acid methyl ester

Guidance literature:: In diethyl ether; at -78 ℃; for 4h;
DOI:10.1021/ja037957x

Reference yield:

: 2-(tert-Butyl-diphenyl-silanyloxy)-6-((2S,4S)-2-methoxymethyl-3,7-dioxa-bicyclo[4.1.0]hept-4-ylmethyl)-benzoic acid methyl ester

: 674336-05-1
2-[(2S,4R,6S)-4-Benzyloxy-6-((S)-2-hydroxy-pent-4-enyl)-tetrahydro-pyran-2-ylmethyl]-6-(tert-butyl-diphenyl-silanyloxy)-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 11 steps

1.1: 74 percent / DIBAL-H / CH₂Cl₂ / 0.67 h / -78 °C

2.1: 70 percent / PPh₃; DIAD / toluene / 16 h / 0 - 25 °C

3.1: 88 percent / 15-crown-5; NaI; BBr₃ / CH₂Cl₂ / 1 h / -30 °C

4.1: 95 percent / 2,6-lutidine / CH₂Cl₂ / 4 h / -78 - 20 °C

5.1: 95 percent / K₂CO₃; methanol / 0.17 h / 20 °C

6.1: 93 percent / TfOH / diethyl ether / 4 h / 20 °C

7.1: 95 percent / HCl / methanol / 0.17 h / 20 °C

8.1: 93 percent / PCC / CH₂Cl₂ / 4 h

9.1: LHMDS / tetrahydrofuran / -78 - 25 °C

9.2: tetrahydrofuran / 18 h / -78 - 25 °C

10.1: 1.19 g / Hg(OAc)2; aq. KI / tetrahydrofuran; H₂O / 0.5 h

11.1: 75 percent / diethyl ether / 4 h / -78 °C

With 2,6-dimethylpyridine; hydrogenchloride; methanol; 15-crown-5; trifluorormethanesulfonic acid; di-isopropyl azodicarboxylate; mercury(II) diacetate; boron tribromide; diisobutylaluminium hydride; potassium carbonate; triphenylphosphine; pyridinium chlorochromate; potassium iodide; sodium iodide; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; toluene; 2.1: Mitsunobu reaction;
DOI:10.1021/ja037957x

Reference yield:

: 674336-01-7
2-(tert-Butyl-diphenyl-silanyloxy)-6-((2S,4S,6R)-4-hydroxy-6-methoxymethyl-tetrahydro-pyran-2-ylmethyl)-benzoic acid methyl ester

: 674336-05-1
2-[(2S,4R,6S)-4-Benzyloxy-6-((S)-2-hydroxy-pent-4-enyl)-tetrahydro-pyran-2-ylmethyl]-6-(tert-butyl-diphenyl-silanyloxy)-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 10 steps

1.1: 70 percent / PPh₃; DIAD / toluene / 16 h / 0 - 25 °C

2.1: 88 percent / 15-crown-5; NaI; BBr₃ / CH₂Cl₂ / 1 h / -30 °C

3.1: 95 percent / 2,6-lutidine / CH₂Cl₂ / 4 h / -78 - 20 °C

4.1: 95 percent / K₂CO₃; methanol / 0.17 h / 20 °C

5.1: 93 percent / TfOH / diethyl ether / 4 h / 20 °C

6.1: 95 percent / HCl / methanol / 0.17 h / 20 °C

7.1: 93 percent / PCC / CH₂Cl₂ / 4 h

8.1: LHMDS / tetrahydrofuran / -78 - 25 °C

8.2: tetrahydrofuran / 18 h / -78 - 25 °C

9.1: 1.19 g / Hg(OAc)2; aq. KI / tetrahydrofuran; H₂O / 0.5 h

10.1: 75 percent / diethyl ether / 4 h / -78 °C

With 2,6-dimethylpyridine; hydrogenchloride; methanol; 15-crown-5; trifluorormethanesulfonic acid; di-isopropyl azodicarboxylate; mercury(II) diacetate; boron tribromide; potassium carbonate; triphenylphosphine; pyridinium chlorochromate; potassium iodide; sodium iodide; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; toluene; 1.1: Mitsunobu reaction;
DOI:10.1021/ja037957x