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2-[7,7-bis(phenylsulfonyl)heptanoyloxy]benzoic acid 5-(3-vinyloxiranyl)pentyl ester

Base Information
  • Chemical Name:2-[7,7-bis(phenylsulfonyl)heptanoyloxy]benzoic acid 5-(3-vinyloxiranyl)pentyl ester
  • CAS No.:1447810-62-9
  • Molecular Formula:C35H40O9S2
  • Molecular Weight:668.829
  • Hs Code.:
2-[7,7-bis(phenylsulfonyl)heptanoyloxy]benzoic acid 5-(3-vinyloxiranyl)pentyl ester

Synonyms:2-[7,7-bis(phenylsulfonyl)heptanoyloxy]benzoic acid 5-(3-vinyloxiranyl)pentyl ester

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Chemical Property of 2-[7,7-bis(phenylsulfonyl)heptanoyloxy]benzoic acid 5-(3-vinyloxiranyl)pentyl ester
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Technology Process of 2-[7,7-bis(phenylsulfonyl)heptanoyloxy]benzoic acid 5-(3-vinyloxiranyl)pentyl ester

There total 10 articles about 2-[7,7-bis(phenylsulfonyl)heptanoyloxy]benzoic acid 5-(3-vinyloxiranyl)pentyl 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:
Guidance literature:
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 0 - 20 ℃; for 12h;
DOI:10.1039/c3ob41020j
Guidance literature:
Multi-step reaction with 4 steps
1.1: sulfuric acid / Reflux
2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1.5 h / Cooling with ice; Schlenk technique; Inert atmosphere
2.2: 60 °C / Inert atmosphere; Schlenk technique
3.1: lithium hydroxide / tetrahydrofuran; methanol / 18 h / 40 °C
3.2: pH 1
4.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 12 h / 0 - 20 °C
With dmap; sulfuric acid; sodium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; mineral oil;
DOI:10.1039/c3ob41020j
Guidance literature:
Multi-step reaction with 6 steps
1.1: sodium hydride / mineral oil; tetrahydrofuran / 2 h / 20 °C
1.2: 20 °C
2.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 1.5 h / -78 °C / Inert atmosphere
2.2: -78 - 20 °C / Inert atmosphere
3.1: sodium hydroxide; benzyltrimethylammonium chloride / methanol; dichloromethane / -20 - 20 °C
4.1: ammonium fluoride / methanol / 8 h / Reflux
5.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0.35 h / Inert atmosphere
5.2: 12 h / 20 °C / Inert atmosphere
6.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 12 h / 0 - 20 °C
With dmap; ammonium fluoride; oxalyl dichloride; di-isopropyl azodicarboxylate; benzyltrimethylammonium chloride; sodium hydride; dimethyl sulfoxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triphenylphosphine; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; mineral oil; 2.1: |Swern Oxidation / 2.2: |Swern Oxidation;
DOI:10.1039/c3ob41020j
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