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Acetic acid 2-benzyloxy-1-benzyloxymethyl-ethylsulfanylmethyl ester

Base Information Edit
  • Chemical Name:Acetic acid 2-benzyloxy-1-benzyloxymethyl-ethylsulfanylmethyl ester
  • CAS No.:97151-26-3
  • Molecular Formula:C20H24O4S
  • Molecular Weight:360.474
  • Hs Code.:
  • Mol file:97151-26-3.mol
Acetic acid 2-benzyloxy-1-benzyloxymethyl-ethylsulfanylmethyl ester

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Chemical Property of Acetic acid 2-benzyloxy-1-benzyloxymethyl-ethylsulfanylmethyl ester Edit
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Technology Process of Acetic acid 2-benzyloxy-1-benzyloxymethyl-ethylsulfanylmethyl ester

There total 4 articles about Acetic acid 2-benzyloxy-1-benzyloxymethyl-ethylsulfanylmethyl 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:
Multi-step reaction with 4 steps
1: 96 percent / pyridine / 16 h / Ambient temperature
2: 94 percent / dimethylformamide / 2 h / 90 °C
3: 54 percent / NH3 / methanol / 16 h / Ambient temperature
4: 1.) HCl gas / 1.) 1,2-dichloroethane, 0 deg C, 2.) DMF, RT, 2 h
With pyridine; hydrogenchloride; ammonia; In methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00147a020
Guidance literature:
Multi-step reaction with 3 steps
1: 94 percent / dimethylformamide / 2 h / 90 °C
2: 54 percent / NH3 / methanol / 16 h / Ambient temperature
3: 1.) HCl gas / 1.) 1,2-dichloroethane, 0 deg C, 2.) DMF, RT, 2 h
With hydrogenchloride; ammonia; In methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00147a020
Guidance literature:
Multi-step reaction with 2 steps
1: 54 percent / NH3 / methanol / 16 h / Ambient temperature
2: 1.) HCl gas / 1.) 1,2-dichloroethane, 0 deg C, 2.) DMF, RT, 2 h
With hydrogenchloride; ammonia; In methanol;
DOI:10.1021/jm00147a020
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