2-Allyl-6-methoxy-benzoic acid (3R,5R)-2-methoxy-5-((S)-1-trifluoromethanesulfonyloxy-ethyl)-tetrahydro-furan-3-yl ester

Base Information

Chemical Name:2-Allyl-6-methoxy-benzoic acid (3R,5R)-2-methoxy-5-((S)-1-trifluoromethanesulfonyloxy-ethyl)-tetrahydro-furan-3-yl ester
CAS No.:865622-63-5
Molecular Formula:C₁₉H₂₃F₃O₈S
Molecular Weight:468.448
Hs Code.:

Synonyms:2-Allyl-6-methoxy-benzoic acid (3R,5R)-2-methoxy-5-((S)-1-trifluoromethanesulfonyloxy-ethyl)-tetrahydro-furan-3-yl ester

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Chemical Property of 2-Allyl-6-methoxy-benzoic acid (3R,5R)-2-methoxy-5-((S)-1-trifluoromethanesulfonyloxy-ethyl)-tetrahydro-furan-3-yl ester

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Technology Process of 2-Allyl-6-methoxy-benzoic acid (3R,5R)-2-methoxy-5-((S)-1-trifluoromethanesulfonyloxy-ethyl)-tetrahydro-furan-3-yl ester

There total 13 articles about 2-Allyl-6-methoxy-benzoic acid (3R,5R)-2-methoxy-5-((S)-1-trifluoromethanesulfonyloxy-ethyl)-tetrahydro-furan-3-yl 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:

: 73-34-7,87-96-7,488-79-9,551-63-3,609-01-8,643-17-4,643-18-5,4164-09-4,6014-42-2,6155-36-8,6189-71-5,6696-41-9,6736-43-2,13224-93-6,22611-09-2,28161-49-1,28161-50-4,28161-52-6,45864-36-6,63814-64-2,71116-59-1,71116-61-5,72598-05-1,87936-88-7,87936-89-8,97466-79-0,116908-82-8,120442-60-6,123484-22-0,133576-32-6
L-rhamnose

: 865622-63-5
2-Allyl-6-methoxy-benzoic acid (3R,5R)-2-methoxy-5-((S)-1-trifluoromethanesulfonyloxy-ethyl)-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 8 steps

1.1: 99 percent / BaCO₃; Br₂ / H₂O / 24 h / 20 °C

2.1: 99 percent / pyridine / 0 - 20 °C

3.1: 99 percent / H₂; Et₃N / Pd/C / ethyl acetate / 24 h / 20 °C / 2585.74 Torr

4.1: NaOMe / methanol / 3 h / 20 °C

4.2: 87 percent / H₂SO₄ / dioxane / 1 h / 20 °C

5.1: 90 percent / EDCI; DMAP / CH₂Cl₂ / 24 h / 20 °C

6.1: DIBAL-H / toluene / 0.25 h / -78 °C

7.1: HCl / dioxane / 4 h / 20 °C

8.1: pyridine / 0.25 h / 0 °C

With pyridine; hydrogenchloride; dmap; hydrogen; bromine; sodium methylate; diisobutylaluminium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; barium carbonate; palladium on activated charcoal; In 1,4-dioxane; methanol; dichloromethane; water; ethyl acetate; toluene;
DOI:10.1021/ol035630v

Reference yield:

: 81644-86-2
2,3,5-tri-O-benzoyl-L-rhamnono-1,4-lactone

: 865622-63-5
2-Allyl-6-methoxy-benzoic acid (3R,5R)-2-methoxy-5-((S)-1-trifluoromethanesulfonyloxy-ethyl)-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: 99 percent / H₂; Et₃N / Pd/C / ethyl acetate / 24 h / 20 °C / 2585.74 Torr

2.1: NaOMe / methanol / 3 h / 20 °C

2.2: 87 percent / H₂SO₄ / dioxane / 1 h / 20 °C

3.1: 90 percent / EDCI; DMAP / CH₂Cl₂ / 24 h / 20 °C

4.1: DIBAL-H / toluene / 0.25 h / -78 °C

5.1: HCl / dioxane / 4 h / 20 °C

6.1: pyridine / 0.25 h / 0 °C

With pyridine; hydrogenchloride; dmap; hydrogen; sodium methylate; diisobutylaluminium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; palladium on activated charcoal; In 1,4-dioxane; methanol; dichloromethane; ethyl acetate; toluene;
DOI:10.1021/ol035630v

Reference yield:

: 20031-16-7
L-Rhamnono-1,4-lactone

: 865622-63-5
2-Allyl-6-methoxy-benzoic acid (3R,5R)-2-methoxy-5-((S)-1-trifluoromethanesulfonyloxy-ethyl)-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: 99 percent / pyridine / 0 - 20 °C

2.1: 99 percent / H₂; Et₃N / Pd/C / ethyl acetate / 24 h / 20 °C / 2585.74 Torr

3.1: NaOMe / methanol / 3 h / 20 °C

3.2: 87 percent / H₂SO₄ / dioxane / 1 h / 20 °C

4.1: 90 percent / EDCI; DMAP / CH₂Cl₂ / 24 h / 20 °C

5.1: DIBAL-H / toluene / 0.25 h / -78 °C

6.1: HCl / dioxane / 4 h / 20 °C

7.1: pyridine / 0.25 h / 0 °C

With pyridine; hydrogenchloride; dmap; hydrogen; sodium methylate; diisobutylaluminium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; palladium on activated charcoal; In 1,4-dioxane; methanol; dichloromethane; ethyl acetate; toluene;
DOI:10.1021/ol035630v