{5-((E)-4-Hydroxy-3-methyl-but-2-enyloxy)-2-[3-(4-methoxycarbonylmethoxy-phenyl)-propionyl]-phenoxy}-acetic acid methyl ester

Base Information

Chemical Name:{5-((E)-4-Hydroxy-3-methyl-but-2-enyloxy)-2-[3-(4-methoxycarbonylmethoxy-phenyl)-propionyl]-phenoxy}-acetic acid methyl ester
CAS No.:98314-78-4
Molecular Formula:C₂₆H₃₀O₉
Molecular Weight:486.519
Hs Code.:

Synonyms:{5-((E)-4-Hydroxy-3-methyl-but-2-enyloxy)-2-[3-(4-methoxycarbonylmethoxy-phenyl)-propionyl]-phenoxy}-acetic acid methyl ester

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Chemical Property of {5-((E)-4-Hydroxy-3-methyl-but-2-enyloxy)-2-[3-(4-methoxycarbonylmethoxy-phenyl)-propionyl]-phenoxy}-acetic acid methyl ester

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Technology Process of {5-((E)-4-Hydroxy-3-methyl-but-2-enyloxy)-2-[3-(4-methoxycarbonylmethoxy-phenyl)-propionyl]-phenoxy}-acetic acid methyl ester

There total 8 articles about {5-((E)-4-Hydroxy-3-methyl-but-2-enyloxy)-2-[3-(4-methoxycarbonylmethoxy-phenyl)-propionyl]-phenoxy}-acetic acid 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: 76.0%

: 56904-88-2
trans-3-hydroxymethyl-2-butenyl chloride

: 98314-74-0
4'-hydroxy-2',4-bis(methoxycarbonylmethoxy)dihydrochalcone

: 98314-78-4
{5-((E)-4-Hydroxy-3-methyl-but-2-enyloxy)-2-[3-(4-methoxycarbonylmethoxy-phenyl)-propionyl]-phenoxy}-acetic acid methyl ester

Guidance literature:: With potassium carbonate; potassium iodide; In acetone; for 10h; Ambient temperature;
DOI:10.1248/cpb.33.1327

Reference yield:

: 89-84-9
2',4'-dihydroxy-4-acetophenone

: 98314-78-4
{5-((E)-4-Hydroxy-3-methyl-but-2-enyloxy)-2-[3-(4-methoxycarbonylmethoxy-phenyl)-propionyl]-phenoxy}-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 80 percent / K₂CO₃ / acetone / 4 h / 50 °C

2: 91 percent / KOH / acetone / 8 h / Ambient temperature

3: 93 percent / H₂ / Pd-C (10percent) / methanol; dioxane

4: 85 percent / NaOH / H₂O; ethanol / 8 h / Ambient temperature

5: 76 percent / concd. HCl / 7 h / Heating

6: 63 percent / H₂ / Pd-C (10percent) / methanol; dioxane

7: 76 percent / K₂CO₃, KI / acetone / 10 h / Ambient temperature

With hydrogenchloride; potassium hydroxide; sodium hydroxide; hydrogen; potassium carbonate; potassium iodide; palladium on activated charcoal; In 1,4-dioxane; methanol; ethanol; water; acetone;
DOI:10.1248/cpb.33.1327

Reference yield:

: 29682-12-0
1-[4-(benzyloxy)-2-hydroxyphenyl]ethanone

: 98314-78-4
{5-((E)-4-Hydroxy-3-methyl-but-2-enyloxy)-2-[3-(4-methoxycarbonylmethoxy-phenyl)-propionyl]-phenoxy}-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 91 percent / KOH / acetone / 8 h / Ambient temperature

2: 93 percent / H₂ / Pd-C (10percent) / methanol; dioxane

3: 85 percent / NaOH / H₂O; ethanol / 8 h / Ambient temperature

4: 76 percent / concd. HCl / 7 h / Heating

5: 63 percent / H₂ / Pd-C (10percent) / methanol; dioxane

6: 76 percent / K₂CO₃, KI / acetone / 10 h / Ambient temperature

With hydrogenchloride; potassium hydroxide; sodium hydroxide; hydrogen; potassium carbonate; potassium iodide; palladium on activated charcoal; In 1,4-dioxane; methanol; ethanol; water; acetone;
DOI:10.1248/cpb.33.1327