Methanesulfonic acid (S)-4-(3-benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester

Base Information

Chemical Name:Methanesulfonic acid (S)-4-(3-benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester
CAS No.:512778-22-2
Molecular Formula:C₁₇H₂₆O₆S
Molecular Weight:358.456
Hs Code.:

Synonyms:Methanesulfonic acid (S)-4-(3-benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Methanesulfonic acid (S)-4-(3-benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester

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Technology Process of Methanesulfonic acid (S)-4-(3-benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester

There total 6 articles about Methanesulfonic acid (S)-4-(3-benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl 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: 87.0%

: 124-63-0
methanesulfonyl chloride

: 512778-21-1
[(R)-4-(3-Benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-methanol

: 512778-22-2
Methanesulfonic acid (S)-4-(3-benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 1h;
DOI:10.1081/NCN-120015727

Reference yield:

: 212763-45-6
(-)-(2R)-2-hydroxy-2-(hydroxymethyl)-2,2'-O-isopropylidenepent-4-enol

: 512778-22-2
Methanesulfonic acid (S)-4-(3-benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 95 percent / imidazole / CH₂Cl₂ / 2 h / 20 °C

2.1: BH₃/DMS / tetrahydrofuran / 20 °C

2.2: 56 percent / NaOH; H₂O₂ / tetrahydrofuran / 2 h / 20 °C

3.1: NaH / tetrahydrofuran / 1 h / 20 °C

3.2: 80 percent / tetrahydrofuran / 20 °C

4.1: 85 percent / tetrabutylammonium fluoride / tetrahydrofuran / 3 h / 20 °C

5.1: 87 percent / Et₃N / CH₂Cl₂ / 1 h / 0 °C

With 1H-imidazole; 2,3-dimercapto-succinic acid; borane; tetrabutyl ammonium fluoride; sodium hydride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1081/NCN-120015727

Reference yield:

: 106267-98-5
(-)-(2S)-2-hydroxy-2-(hydroxymethyl)-2,2'-O-isopropylidenepent-4-enoic acid

: 512778-22-2
Methanesulfonic acid (S)-4-(3-benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: 88 percent / LiAlH₄ / tetrahydrofuran / Heating

2.1: 95 percent / imidazole / CH₂Cl₂ / 2 h / 20 °C

3.1: BH₃/DMS / tetrahydrofuran / 20 °C

3.2: 56 percent / NaOH; H₂O₂ / tetrahydrofuran / 2 h / 20 °C

4.1: NaH / tetrahydrofuran / 1 h / 20 °C

4.2: 80 percent / tetrahydrofuran / 20 °C

5.1: 85 percent / tetrabutylammonium fluoride / tetrahydrofuran / 3 h / 20 °C

6.1: 87 percent / Et₃N / CH₂Cl₂ / 1 h / 0 °C

With 1H-imidazole; lithium aluminium tetrahydride; 2,3-dimercapto-succinic acid; borane; tetrabutyl ammonium fluoride; sodium hydride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1081/NCN-120015727