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3-(2-Methoxycarbonylmethoxyphenyl)acrylic acid methyl

Base Information
  • Chemical Name:3-(2-Methoxycarbonylmethoxyphenyl)acrylic acid methyl
  • CAS No.:76268-12-7
  • Molecular Formula:C13H14O5
  • Molecular Weight:250.251
  • Hs Code.:
3-(2-Methoxycarbonylmethoxyphenyl)acrylic acid methyl

Synonyms:

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Chemical Property of 3-(2-Methoxycarbonylmethoxyphenyl)acrylic acid methyl
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Technology Process of 3-(2-Methoxycarbonylmethoxyphenyl)acrylic acid methyl

There total 1 articles about 3-(2-Methoxycarbonylmethoxyphenyl)acrylic acid methyl 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:
Guidance literature:
methanol; coumarin; With sodium methylate; for 0.166667h; Heating;
bromoacetic acid methyl ester; for 3.5h; Further stages.; Heating;
DOI:10.1039/b000619j
Guidance literature:
Multi-step reaction with 4 steps
1: 68 percent / NaOMe / methanol / 0.25 h / 70 °C
2: 80 percent / N-bromosuccinimide; dibenzoyl peroxide / CCl4 / 5 h / Heating
3: 97 percent / DBU / CH2Cl2 / 1.5 h / 20 °C
4: 25 percent / p-TsOH / 14 h / Heating
With N-Bromosuccinimide; sodium methylate; toluene-4-sulfonic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; dibenzoyl peroxide; In methanol; tetrachloromethane; dichloromethane; 1: Cyclization / 2: Bromination / 3: Elimination / 4: Esterification;
DOI:10.1039/b000619j
Guidance literature:
Multi-step reaction with 5 steps
1: 68 percent / NaOMe / methanol / 0.25 h / 70 °C
2: 80 percent / N-bromosuccinimide; dibenzoyl peroxide / CCl4 / 5 h / Heating
3: 56 percent / K2CO3; H2O / methanol / 15 h / 20 °C
4: acetyl chloride / benzene / 5 h
5: 4 h / Heating
With N-Bromosuccinimide; water; sodium methylate; potassium carbonate; acetyl chloride; dibenzoyl peroxide; In methanol; tetrachloromethane; benzene; 1: Cyclization / 2: Bromination / 3: Hydrolysis / 4: Cyclization / 5: Esterification;
DOI:10.1039/b000619j
upstream raw materials:

methanol

coumarin

bromoacetic acid methyl ester

Downstream raw materials:

methyl 2-carboxybenzofuran-3-acetate

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