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17α-p-bromobenzoyloxy-4,6-pregnadiene-3,20-dione

Base Information Edit
  • Chemical Name:17α-p-bromobenzoyloxy-4,6-pregnadiene-3,20-dione
  • CAS No.:1190878-48-8
  • Molecular Formula:C28H31BrO4
  • Molecular Weight:511.456
  • Hs Code.:
  • Mol file:1190878-48-8.mol
17α-p-bromobenzoyloxy-4,6-pregnadiene-3,20-dione

Synonyms:17α-p-bromobenzoyloxy-4,6-pregnadiene-3,20-dione

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Chemical Property of 17α-p-bromobenzoyloxy-4,6-pregnadiene-3,20-dione Edit
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Technology Process of 17α-p-bromobenzoyloxy-4,6-pregnadiene-3,20-dione

There total 3 articles about 17α-p-bromobenzoyloxy-4,6-pregnadiene-3,20-dione 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:
4-Bromobenzoic acid; With toluene-4-sulfonic acid; trifluoroacetic anhydride; In chloroform; at 20 ℃; for 0.5h;
17α-hydroxypregna-4,6-diene-3,20-dione; In chloroform; at 20 ℃; for 2h;
DOI:10.1016/j.steroids.2009.04.009
Guidance literature:
Multi-step reaction with 2 steps
1: sodium hydroxide / methanol / 2 h / Reflux
2: toluene-4-sulfonic acid; trifluoroacetic anhydride / chloroform / 3 h
With toluene-4-sulfonic acid; trifluoroacetic anhydride; sodium hydroxide; In methanol; chloroform; 2: |Steglich Esterification;
DOI:10.1016/j.ejmech.2014.06.008
Guidance literature:
Multi-step reaction with 3 steps
1: sodium hydroxide; chloranil / toluene; acetic acid / 4 h / Reflux
2: sodium hydroxide / methanol / 2 h / Reflux
3: toluene-4-sulfonic acid; trifluoroacetic anhydride / chloroform / 3 h
With chloranil; toluene-4-sulfonic acid; trifluoroacetic anhydride; sodium hydroxide; In methanol; chloroform; acetic acid; toluene; 3: |Steglich Esterification;
DOI:10.1016/j.ejmech.2014.06.008
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