(R)-1-{(4S,5S)-5-[(E)-3-{[(allyloxy)carbonyl]oxy}-2-methylbuta-1,3-dien-1-yl]-2,2-dimethyl-1,3-dioxolan-4-yl}-3-methylbut-3-en-2-yl benzoate

Base Information

Chemical Name:(R)-1-{(4S,5S)-5-[(E)-3-{[(allyloxy)carbonyl]oxy}-2-methylbuta-1,3-dien-1-yl]-2,2-dimethyl-1,3-dioxolan-4-yl}-3-methylbut-3-en-2-yl benzoate
CAS No.:1429033-80-6
Molecular Formula:C₂₆H₃₂O₇
Molecular Weight:456.536
Hs Code.:

Synonyms:(R)-1-{(4S,5S)-5-[(E)-3-{[(allyloxy)carbonyl]oxy}-2-methylbuta-1,3-dien-1-yl]-2,2-dimethyl-1,3-dioxolan-4-yl}-3-methylbut-3-en-2-yl benzoate

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Chemical Property of (R)-1-{(4S,5S)-5-[(E)-3-{[(allyloxy)carbonyl]oxy}-2-methylbuta-1,3-dien-1-yl]-2,2-dimethyl-1,3-dioxolan-4-yl}-3-methylbut-3-en-2-yl benzoate

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Technology Process of (R)-1-{(4S,5S)-5-[(E)-3-{[(allyloxy)carbonyl]oxy}-2-methylbuta-1,3-dien-1-yl]-2,2-dimethyl-1,3-dioxolan-4-yl}-3-methylbut-3-en-2-yl benzoate

There total 6 articles about (R)-1-{(4S,5S)-5-[(E)-3-{[(allyloxy)carbonyl]oxy}-2-methylbuta-1,3-dien-1-yl]-2,2-dimethyl-1,3-dioxolan-4-yl}-3-methylbut-3-en-2-yl benzoate 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: 71.0%

: 1429033-75-9
(R)-1-{(4S,5S)-2,2-dimethyl-5-[(E)-2-methyl-3-oxobut-1-en-1-yl]-1,3-dioxolan-4-yl}-3-methylbut-3-en-2-yl benzoate

: 2937-50-0
Allyl chloroformate

: 1429033-80-6
(R)-1-{(4S,5S)-5-[(E)-3-{[(allyloxy)carbonyl]oxy}-2-methylbuta-1,3-dien-1-yl]-2,2-dimethyl-1,3-dioxolan-4-yl}-3-methylbut-3-en-2-yl benzoate

Guidance literature:: (R)-1-{(4S,5S)-2,2-dimethyl-5-[(E)-2-methyl-3-oxobut-1-en-1-yl]-1,3-dioxolan-4-yl}-3-methylbut-3-en-2-yl benzoate; With potassium hexamethylsilazane; In 1,2-dimethoxyethane; at -78 ℃; for 0.0833333h; Inert atmosphere;

Allyl chloroformate; In 1,2-dimethoxyethane; at 0 ℃; for 1h; Inert atmosphere;
DOI:10.1021/jo400029u

Reference yield:

: 1429033-74-8
(R)-1-[(4S,5S)-5-(hydroxymethyl)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-methylbut-3-en-2-yl benzoate

: 1429033-80-6
(R)-1-{(4S,5S)-5-[(E)-3-{[(allyloxy)carbonyl]oxy}-2-methylbuta-1,3-dien-1-yl]-2,2-dimethyl-1,3-dioxolan-4-yl}-3-methylbut-3-en-2-yl benzoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 3 h / 20 °C / Inert atmosphere

2.1: sodium hydride / tetrahydrofuran; mineral oil / 1 h / 0 °C / Inert atmosphere

2.2: 14 h / 20 °C / Inert atmosphere

3.1: potassium hexamethylsilazane / 1,2-dimethoxyethane / 0.08 h / -78 °C / Inert atmosphere

3.2: 1 h / 0 °C / Inert atmosphere

With potassium hexamethylsilazane; sodium hydride; sodium hydrogencarbonate; Dess-Martin periodane; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; mineral oil;
DOI:10.1021/jo400029u

Reference yield:

: C₃₄H₄₂O₅Si

: 1429033-80-6
(R)-1-{(4S,5S)-5-[(E)-3-{[(allyloxy)carbonyl]oxy}-2-methylbuta-1,3-dien-1-yl]-2,2-dimethyl-1,3-dioxolan-4-yl}-3-methylbut-3-en-2-yl benzoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrabutyl ammonium fluoride; acetic acid / tetrahydrofuran / 3 h / 20 °C / Inert atmosphere

2.1: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 3 h / 20 °C / Inert atmosphere

3.1: sodium hydride / tetrahydrofuran; mineral oil / 1 h / 0 °C / Inert atmosphere

3.2: 14 h / 20 °C / Inert atmosphere

4.1: potassium hexamethylsilazane / 1,2-dimethoxyethane / 0.08 h / -78 °C / Inert atmosphere

4.2: 1 h / 0 °C / Inert atmosphere

With tetrabutyl ammonium fluoride; potassium hexamethylsilazane; sodium hydride; sodium hydrogencarbonate; Dess-Martin periodane; acetic acid; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; mineral oil;
DOI:10.1021/jo400029u