Dichloromethane → 3-(3-Pentyl)benzyl alcohol

Temperature

0 °C

A 250 mL round bottomed flask equipped with a nitrogen inlet and a magnetic stirrer was charged with 3.9 g of 3-(3-hydroxy-3-pentyl)-O-(tert-butyltrimethylsilyl)benzyl alcohol and 25 mL of CH2Cl2. The solution was cooled to 0° C. in an ice bath and was treated with 15 mL of TFA followed by 5 mL of Et3SiH (Aldrich). After 30 min at 0° C. the ice bath was removed and the solution was stirred at RT for 18 h. The solution was concentrated to a viscous liquid. This material was dissolved in ether (60 mL), washed with 5% aqueous NaHCO3 (3×50 mL), dried over anhydrous MgSO4, and concentrated in vacuo. The resulting liquid was dissolved in 10 mL of THF and treated with 63 mL of 1M Bu4NF/THF (Aldrich). After stirring at RT for 18 h, the solution was concentrated and the resulting syrup mixed with 80 mL of water. The mixture was extracted with ether (4×30 mL). The combined extracts were washed with 5% aqueous NaHCO3 (3×50 mL), dried over anhydrous MgSO4, and concentrated to afford a light yellow liquid. Analysis by tlc (SiO2, 9:1 hexane:EtOAc) indicated a major new component at Rf =0.30. The crude product was purified by flash chromatography on silica gel (85:15 hexane:EtOAc) to give 1.84 g (82%) of 3-(3-pentyl)benzyl alcohol as a clear liquid. 1H-NMR: (300 MHz, DMSO-d6) δ 7.21 (t, 1H, J=7.5, aromatic CH), 7.10 (m, 2H, aromatic CH), 6.99 (d, 1H, J=7.4, aromatic CH), 5.12 (t, 1H, J=5.8, OH), 4.46 (d, 2H, J=5.8, ArCH2O), 2.26 (m, 1H, pentyl methine), 1.62 (m, 2H, pentyl CH2), 1.49 (m, 2H, pentyl CH2), 0.69 (t, 6H, J=7.4, pentyl CH3).

1. customA 250 mL round bottomed flask equipped with a nitrogen inlet and a magnetic stirrer
2. customAfter 30 min at 0° C. the ice bath was removed
3. concentrationThe solution was concentrated to a viscous liquid
4. dissolutionThis material was dissolved in ether (60 mL)
5. washwashed with 5% aqueous NaHCO3 (3×50 mL)
6. dry with materialdried over anhydrous MgSO4
7. concentrationconcentrated in vacuo
8. dissolutionThe resulting liquid was dissolved in 10 mL of THF
9. additiontreated with 63 mL of 1M Bu4NF/THF (Aldrich)
10. stirringAfter stirring at RT for 18 h
11. concentrationthe solution was concentrated
12. additionthe resulting syrup mixed with 80 mL of water
13. extractionThe mixture was extracted with ether (4×30 mL)
14. washThe combined extracts were washed with 5% aqueous NaHCO3 (3×50 mL)
15. dry with materialdried over anhydrous MgSO4
16. concentrationconcentrated
17. customto afford a light yellow liquid
18. customThe crude product was purified by flash chromatography on silica gel (85:15 hexane:EtOAc)

ORD record

ord-c58df7ade4ce4191ba90931e7efd1c91

Source dataset

uspto-grants-2000_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06140100