Chlorohydroquinone → (R)-3-(2-Chlorophenoxy)-pyrrolidine HCl

Diisopropyl azodicarboxylate (21 mL, 107 mmol) and 4-hydroxy-3-chlorophenol (11.1 mL, 107 mmol) were added portionwise to an ice-cold solution of tert-butyl (3S)-3-hydroxypyrrolidine-1-carboxylate (20 g, 107 mmol) and triphenylphosphine (28.1 g, 107 mmol) in tetrahydrofuran (320 mL) and the mixture was stirred at room temperature for 18 hours. The reaction mixture was then concentrated in vacuo and the residue was treated with hydrochloric acid (4M in dioxane, 250 mL). The mixture was concentrated in vacuo and the residue was partitioned between ethyl acetate (400 mL) and water (400 mL). The organic layer was separated and washed with water (100 mL), and the combined aqueous solution was washed with ethyl acetate (2×300 mL), basified to pH9 with solid potassium carbonate and extracted with ethyl acetate (2×400 mL). The combined organic solution was then washed with water (3×300 mL), dried over magnesium sulfate and concentrated in vacuo. The residual oil was dissolved in diethyl ether (60 mL), treated dropwise with hydrochloric acid (4M in dioxane, 25 mL) and the resulting precipitate was filtered off, washing through with diethyl ether, and dried to afford the title compound as a white solid in 55% yield, 13.69 g. LRMS APCI m/z 198 [M+H]+

1. concentrationThe reaction mixture was then concentrated in vacuo
2. additionthe residue was treated with hydrochloric acid (4M in dioxane, 250 mL)
3. concentrationThe mixture was concentrated in vacuo
4. customthe residue was partitioned between ethyl acetate (400 mL) and water (400 mL)
5. customThe organic layer was separated
6. washwashed with water (100 mL)
7. washthe combined aqueous solution was washed with ethyl acetate (2×300 mL)
8. extractionextracted with ethyl acetate (2×400 mL)
9. washThe combined organic solution was then washed with water (3×300 mL)
10. dry with materialdried over magnesium sulfate
11. concentrationconcentrated in vacuo
12. dissolutionThe residual oil was dissolved in diethyl ether (60 mL)
13. additiontreated dropwise with hydrochloric acid (4M in dioxane, 25 mL)
14. filtrationthe resulting precipitate was filtered off
15. washwashing through with diethyl ether
16. customdried

ORDレコード

ord-5182725d11b14ce8a73c83749b8f9b2f

出典データセット

uspto-grants-2012_06

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08207198B2