2-O-methyllecanoric acid

Base Information

Chemical Name:2-O-methyllecanoric acid
CAS No.:219700-70-6
Molecular Formula:C₂₄H₂₂O₇
Molecular Weight:422.434
Hs Code.:

Synonyms:2-O-methyllecanoric acid

Suppliers and Price of 2-O-methyllecanoric acid

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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 2-O-methyllecanoric acid

Chemical Property:

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Technology Process of 2-O-methyllecanoric acid

There total 4 articles about 2-O-methyllecanoric acid 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: 82.0%

: 219700-72-8
2-hydroxy-4-[(4-hydroxy-2-methoxy-6-methylbenzoyl)oxy]-6-methylbenzoic acid

: 100-39-0
benzyl bromide

: 219700-70-6
2-O-methyllecanoric acid

Guidance literature:: With potassium hydrogencarbonate; In N,N-dimethyl-formamide; for 24h; Ambient temperature;
DOI:10.1071/C98082

Reference yield:

: 38862-71-4
benzyl 2,4-dihydroxy-6-methylbenzoate

: 219700-70-6
2-O-methyllecanoric acid

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / dicyclohexylcabodiimide / toluene; diethyl ether / 12 h

2: 90 percent / hydrogen / 10 percent palladium on carbon / ethyl acetate / 16 h

3: 82 percent / potassium hydrogen carbonate / dimethylformamide / 24 h / Ambient temperature

With hydrogen; potassium hydrogencarbonate; dicyclohexyl-carbodiimide; palladium on activated charcoal; In diethyl ether; ethyl acetate; N,N-dimethyl-formamide; toluene;
DOI:10.1071/C98082

Reference yield:

: 22375-06-0
4-benzyloxy-2-methoxy-6-methylbenzoic acid

: 219700-70-6
2-O-methyllecanoric acid

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / dicyclohexylcabodiimide / toluene; diethyl ether / 12 h

2: 90 percent / hydrogen / 10 percent palladium on carbon / ethyl acetate / 16 h

3: 82 percent / potassium hydrogen carbonate / dimethylformamide / 24 h / Ambient temperature

With hydrogen; potassium hydrogencarbonate; dicyclohexyl-carbodiimide; palladium on activated charcoal; In diethyl ether; ethyl acetate; N,N-dimethyl-formamide; toluene;
DOI:10.1071/C98082