反应 #78037

ord-d01a7072414048f0959f8877f8c7fd94

反应方程式

C[C@]12CCC(=O)C(Cl)=C1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O)C[C@@H]3C[C@]312
4-Chloro-17β-hydroxy-14α,15α-methylene-androst-4-ene-3-one
Br
hydrobromic acid
→
C[C@]12CCC(=O)C(Br)=C1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O)C[C@@H]3C[C@]312
4-Bromo-17β-hydroxy-14α,15α-methylene-androst-4-ene-3-one

反应物

C[C@]12CCC(=O)C(Cl)=C1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O)C[C@@H]3C[C@]312
4-Chloro-17β-hydroxy-14α,15α-methylene-androst-4-ene-3-one
Br
hydrobromic acid

试剂

无

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

The target compound is synthesized in a manner similar to the synthesis of 4-Chloro-17β-hydroxy-14α,15α-methylene-androst-4-ene-3-one, 48% hydrobromic acid being used instead of hydrochloric acid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06710039B1uspto-grants-2004_03