Reaction #459709

ord-22b35a01fdee480692885be2f2b2a262

Reaction equation

CC(=O)OC(CCCCl)CCCCC(F)(F)F
1-chloro-4-acetoxy-9,9,9-trifluorononane
CCOC(=O)CCCCCCN(CCCC(CCCCC(F)(F)F)OC(C)=O)S(C)(=O)=O
ethyl 7-[N-(4-acetoxy-9,9,9-trifluorononyl)methanesulfonamido]heptanoate
→
CCCCC[C@@H](O)C#CCN(CCCCCCC(=O)O)S(C)(=O)=O
7-[N-(4-hydroxy-9,9,9-trifluorononyl)methanesulfonamido]heptanoic acid
CCCCC[C@@H](O)C#CCN(CCCCCCC(=O)O)S(C)(=O)=O
7-[N-(4(R)-hydroxy-2-nonynyl)methanesulfonamido]heptanoic acid

Reactants

CC(=O)OC(CCCCl)CCCCC(F)(F)F
1-chloro-4-acetoxy-9,9,9-trifluorononane
—
product
CCOC(=O)CCCCCCN(CCCC(CCCCC(F)(F)F)OC(C)=O)S(C)(=O)=O
ethyl 7-[N-(4-acetoxy-9,9,9-trifluorononyl)methanesulfonamido]heptanoate

Reagents

None

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherThe synthesis of this compound

Procedure

The synthesis of this compound is carried out as described in Example 1, except that, in Step A, the 1-chloro-4-acetoxy-9,9,9-trifluorononane (Example E). The product of Step A is thus ethyl 7-[N-(4-acetoxy-9,9,9-trifluorononyl)methanesulfonamido]heptanoate. The subsequent step yields 7-[N-(4-hydroxy-9,9,9-trifluorononyl)methanesulfonamido]heptanoic acid (B).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04091107uspto-grants-1978_05