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(1R,2S)-1-(4-methoxybenzyloxymethyl)-2-hydroxypent-4-enyl hex-5-enoate

Base Information
  • Chemical Name:(1R,2S)-1-(4-methoxybenzyloxymethyl)-2-hydroxypent-4-enyl hex-5-enoate
  • CAS No.:475055-37-9
  • Molecular Formula:C20H28O5
  • Molecular Weight:348.439
  • Hs Code.:
(1R,2S)-1-(4-methoxybenzyloxymethyl)-2-hydroxypent-4-enyl hex-5-enoate

Synonyms:(1R,2S)-1-(4-methoxybenzyloxymethyl)-2-hydroxypent-4-enyl hex-5-enoate

Suppliers and Price of (1R,2S)-1-(4-methoxybenzyloxymethyl)-2-hydroxypent-4-enyl hex-5-enoate
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Chemical Property of (1R,2S)-1-(4-methoxybenzyloxymethyl)-2-hydroxypent-4-enyl hex-5-enoate
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Technology Process of (1R,2S)-1-(4-methoxybenzyloxymethyl)-2-hydroxypent-4-enyl hex-5-enoate

There total 3 articles about (1R,2S)-1-(4-methoxybenzyloxymethyl)-2-hydroxypent-4-enyl hex-5-enoate 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:
Multi-step reaction with 3 steps
1: 96 percent / camphorsulfonic acid / CH2Cl2 / 18 h / 20 °C
2: 75 percent / diisopropylcarbodiimide; 4-dimethylaminopyridine / CH2Cl2 / 24 h
3: 65 percent / NaBH3CN; molecular sieves 3 Angstroem; HCl / tetrahydrofuran; diethyl ether / 0.5 h / 20 °C
With hydrogenchloride; dmap; 3 A molecular sieve; camphor-10-sulfonic acid; sodium cyanoborohydride; diisopropyl-carbodiimide; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1002/1615-4169(200208)344:6/7<657::AID-ADSC657>3.0.CO;2-0
Guidance literature:
Multi-step reaction with 2 steps
1: 75 percent / diisopropylcarbodiimide; 4-dimethylaminopyridine / CH2Cl2 / 24 h
2: 65 percent / NaBH3CN; molecular sieves 3 Angstroem; HCl / tetrahydrofuran; diethyl ether / 0.5 h / 20 °C
With hydrogenchloride; dmap; 3 A molecular sieve; sodium cyanoborohydride; diisopropyl-carbodiimide; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1002/1615-4169(200208)344:6/7<657::AID-ADSC657>3.0.CO;2-0
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