2-allyl-6-methoxymethoxy-benzoic acid (1R,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4,7-dimethyl-oct-6-enyl ester

Base Information

Chemical Name:2-allyl-6-methoxymethoxy-benzoic acid (1R,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4,7-dimethyl-oct-6-enyl ester
CAS No.:312962-24-6
Molecular Formula:C₃₄H₄₈O₈
Molecular Weight:584.75
Hs Code.:

Synonyms:2-allyl-6-methoxymethoxy-benzoic acid (1R,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4,7-dimethyl-oct-6-enyl ester

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Chemical Property of 2-allyl-6-methoxymethoxy-benzoic acid (1R,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4,7-dimethyl-oct-6-enyl ester

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Technology Process of 2-allyl-6-methoxymethoxy-benzoic acid (1R,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4,7-dimethyl-oct-6-enyl ester

There total 17 articles about 2-allyl-6-methoxymethoxy-benzoic acid (1R,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4,7-dimethyl-oct-6-enyl 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: 84.0%

: 107-30-2
chloromethyl methyl ether

: 312962-21-3
2-allyl-6-hydroxy-benzoic acid (1R,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4,7-dimethyl-oct-6-enyl ester

: 312962-24-6
2-allyl-6-methoxymethoxy-benzoic acid (1R,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4,7-dimethyl-oct-6-enyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; for 18h;
DOI:10.1021/ol006646d

Reference yield:

: 154714-19-9
5-hydroxy-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-one

: 312962-24-6
2-allyl-6-methoxymethoxy-benzoic acid (1R,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4,7-dimethyl-oct-6-enyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 85 percent / pyridine

2: 83 percent / KOMe / PdCl₂(dppf) / tetrahydrofuran

3: 96 percent / BCl₃ / CH₂Cl₂ / 5 h / 20 °C

4: 88 percent / DEAD; PPh₃ / diethyl ether / 20 h / 20 °C

5: 84 percent / diisopropylethylamine / CH₂Cl₂ / 18 h

With pyridine; potassium methanolate; boron trichloride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; diethylazodicarboxylate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; diethyl ether; dichloromethane; 1: Substitution / 2: Substitution / 3: Ring cleavage / 4: Esterification / 5: Alkylation;
DOI:10.1021/ol006646d

Reference yield:

: 303-07-1
2,6-Dihydroxybenzoic acid

: 312962-24-6
2-allyl-6-methoxymethoxy-benzoic acid (1R,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4,7-dimethyl-oct-6-enyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 96 percent / SOCl₂; DMAP / 1,2-dimethoxy-ethane

2: 85 percent / pyridine

3: 83 percent / KOMe / PdCl₂(dppf) / tetrahydrofuran

4: 96 percent / BCl₃ / CH₂Cl₂ / 5 h / 20 °C

5: 88 percent / DEAD; PPh₃ / diethyl ether / 20 h / 20 °C

6: 84 percent / diisopropylethylamine / CH₂Cl₂ / 18 h

With pyridine; dmap; thionyl chloride; potassium methanolate; boron trichloride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; diethylazodicarboxylate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,2-dimethoxyethane; diethyl ether; dichloromethane; 1: Cyclization / 2: Substitution / 3: Substitution / 4: Ring cleavage / 5: Esterification / 6: Alkylation;
DOI:10.1021/ol006646d