Triphenylphosphine → t-butyl (R)-4-(2-acetyl-5-(3-pyridylmethoxy)phenoxy)-4-(2-methylphenyl)butanoate

Diisopropyl azodicarboxylate (8 g) is added portionwise to a stirred solution of triphenylphosphine (10.5 g) in THF (100 mL) at 0° C. under nitrogen. Stirring is continued at 0° C. for 15 minutes. A solution of 2-acetyl-5-(3-pyridylmethoxy)phenol (4.5 g) and tert-butyl (S)-4-hydroxy-4-(2-methylphenyl)butanoate (4.9 g) in THF (100 mL) is added at such a rate that the temperature does not exceed 5° C. The reaction is allowed to warm to ambient temperature stirred for 16 hours, then concentrated in vacuo. The residue is partitioned between ethyl acetate (200 mL) and water (200 mL) and the organic phase dried over magnesium sulphate, filtered and concentrated in vacuo.The residue is purified by flash chromatography on silica eluting initially with a mixture of ethyl acetate and cyclohexane (1:1 v/v) then with ethyl acetate. Fractions homogeneous in the required product are combined and evaporated to give t-butyl (R)-4-(2-acetyl-5-(3-pyridylmethoxy)phenoxy)-4-(2-methylphenyl)butanoate (2 g).

1. customdoes not exceed 5° C
2. stirringstirred for 16 hours
3. concentrationconcentrated in vacuo
4. customThe residue is partitioned between ethyl acetate (200 mL) and water (200 mL)
5. dry with materialthe organic phase dried over magnesium sulphate
6. filtrationfiltered
7. concentrationconcentrated in vacuo.The residue
8. customis purified by flash chromatography on silica eluting initially with a mixture of ethyl acetate and cyclohexane (1:1 v/v)
9. customevaporated

ORDレコード

ord-8546cd1c87444010aa3d6fb0f3952cae

出典データセット

uspto-grants-2001_04

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06211234B1