Tetrahydrofuran → HCID 178453956, 화합물

Methyl trans-4-(tert-butoxycarbonylamino)cyclohexanecarboxylate (55.5 g, 216 mmol) was suspended in ethanol (900 ml) and THF (100 ml) and the mixture was cooled to 5° C. Granular calcium chloride (47.9 g, 431 mmol) was added portionwise to give a milky suspension. Sodium borohydride (32.6 g, 863 mmol) was added portionwise over 25 mins at 5° C. The reaction mixture (white emulsion) was stirred at 5° C. for 1 hour, the water bath was removed and then the reaction mixture was allowed to warm to room temperature and stirred at room temperature overnight. The reaction mixture was cooled to 10° C. and 5% potassium carbonate (200 ml) was added dropwise until the pH of the solution was pH11. A colourless precipitate formed which was filtered off. The solid was stirred with ethyl acetate (2000 ml) and water (500 ml). The organic layer was separated and washed with 0.5M HCl (200 ml), then washed with water (2×200 ml) and saturated brine (100 ml). The organic solution was dried over anhydrous MgSO4, filtered and evaporated to give a white solid. The solid was dried under high vacuum overnight to constant weight; [M+H]+230.

1. customto give a milky suspension
2. customthe water bath was removed
3. temperatureto warm to room temperature
4. stirringstirred at room temperature overnight
5. temperatureThe reaction mixture was cooled to 10° C.
6. addition5% potassium carbonate (200 ml) was added dropwise until the pH of the solution
7. customA colourless precipitate formed which
8. filtrationwas filtered off
9. stirringThe solid was stirred with ethyl acetate (2000 ml) and water (500 ml)
10. customThe organic layer was separated
11. washwashed with 0.5M HCl (200 ml)
12. washwashed with water (2×200 ml) and saturated brine (100 ml)
13. dry with materialThe organic solution was dried over anhydrous MgSO4
14. filtrationfiltered
15. customevaporated
16. customto give a white solid
17. customThe solid was dried under high vacuum overnight to constant weight

ORD 기록

ord-49c60ffbea914a059ceadb4877facf77

출처 데이터셋

uspto-grants-2014_09

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US08835444B2