Diisobutylaluminum hydride → HCID 69285541, compound

Temperature

-78 °C

A solution of (7-Oxo-6-oxa-bicyclo[3.2.1]oct-2-yl)-carbamic acid benzyl ester (2.26 g, 8.2 mmol) in toluene (80 mL) was cooled to −78° C. and treated dropwise with DIBAL-H (11 mL of a 1.0 M toluene solution). The reaction mixture was stirred for 2 h at −78° C. and quenched with 50 mL of 1 N HCl. The mixture was allowed to warm to RT and then extracted with EtOAc (1×). The organic phase was washed with half-saturated brine. The combined aqueoues phases were back extracted with EtOAc (1×). The organic extracts were combined, washed with brine, dried (MgSO4), filtered, and concentrated in vacuo to afford a colorless oil. This material was dissolved in THF (100 mL). The resultant solution was cooled to 0° C. and charged successively with ethyltriphenylphosphonium iodide (5.3 g, 12.3 mmol) and KHMDS (49 mL of a 0.5 M solution in toluene). The ice bath was removed and the reaction was stirred for 4 h at RT before being quenched with the addition of 1 N HCl (50 mL). The biphasic mixture was partitioned between 1 N HCl (50 mL) and EtOAc (50 mL). The aqueous phase was extracted with EtOAc (2×). The organic extracts were combined, washed with brine, dried (MgSO4), filtered, and concentrated in vacuo. Purification of the residue via flash chromatography afforded the desired [(1S,2R,4R)-(4-hydroxy-2-propenyl-cyclohexyl)]-carbamic acid benzyl ester as a colorless oil (0.56 g). MS found: (M+H)+=312.26.

1. customquenched with 50 mL of 1 N HCl
2. temperatureto warm to RT
3. extractionextracted with EtOAc (1×)
4. washThe organic phase was washed with half-saturated brine
5. extractionThe combined aqueoues phases were back extracted with EtOAc (1×)
6. washwashed with brine
7. dry with materialdried (MgSO4)
8. filtrationfiltered
9. concentrationconcentrated in vacuo
10. customto afford a colorless oil
11. customThe ice bath was removed
12. stirringthe reaction was stirred for 4 h at RT
13. custombefore being quenched with the addition of 1 N HCl (50 mL)
14. customThe biphasic mixture was partitioned between 1 N HCl (50 mL) and EtOAc (50 mL)
15. extractionThe aqueous phase was extracted with EtOAc (2×)
16. washwashed with brine
17. dry with materialdried (MgSO4)
18. filtrationfiltered
19. concentrationconcentrated in vacuo
20. customPurification of the residue via flash chromatography

ORD record

ord-83d2fe9ac03d4290bdc2739650573fd3

Source dataset

uspto-grants-2008_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07378409B2