Dimethyl Sulfoxide → (R)-2-(Trityl-amino)-butyraldehyde

温度

-45 °C

To a stirred solution of DMSO (3.0 mL, 2.8 eq, 42.28 mmol) in DCM (30 mL) under an argon atmosphere at −45° C., was added oxalyl chloride (2 M in DCM, 10.56 mL, 1.40 eq, 21.12 mmol), dropwise. The reaction mixture was stirred at −45° C. for 1 h, after which time a solution of (R)-2-(trityl-amino)-butan-1-ol (5 g, 1 eq, 15.08 mmol) in DCM (30 mL) was added dropwise with stirring. The reaction mixture was stirred at this temperature for 3 h, when TLC (hexane:ether; 80:20) indicated that the reaction had gone to completion. To the reaction mixture was added a solution of TEA (10.5 mL, 5 eq, 75.33 mmol) in DCM (30 mL), and the solution allowed to warm to room temperature over 16 h. The reaction mixture was diluted with more DCM (200 mL) and washed with water (250 mL). The aqueous phase was extracted with DCM (3×50 mL), and the combined organic phase washed with brine (50 mL), dried (MgSO4) and evaporated in vacuo. The residue was dissolved in ether (30 mL), the solid precipitate removed by filtration and the filtrate was evaporated in vacuo. The residue was dissolved in hexane (50 mL), the solid precipitate removed by filtration and the filtrate was evaporated in vacuo to afford the title compound as a light yellow oil. Yield: 2.59 g (52%). 1H-NMR (d6-DMSO, 250 MHz): δ 0.77 (t, 3H, J=7.42 Hz, —NHCH(CH2CH3)CHO), 1.34-1.61 (m, 2H, —NHCH(CH2CH3)CHO), 2.92 (m, 1H, —NHCH(CH2CH3)CHO), 3.62 (d, 1H, J=8.21 Hz, —NHCH(CH2CH3)CHO), 7.16-7.46 (m, 15H, 3×Ph), 8.77 (d, 1H, J=3.00 Hz, —NHCH(CH2CH3)CHO).

1. stirringwith stirring
2. stirringThe reaction mixture was stirred at this temperature for 3 h
3. temperatureto warm to room temperature over 16 h
4. washwashed with water (250 mL)
5. extractionThe aqueous phase was extracted with DCM (3×50 mL)
6. washthe combined organic phase washed with brine (50 mL)
7. dry with materialdried (MgSO4)
8. customevaporated in vacuo
9. dissolutionThe residue was dissolved in ether (30 mL)
10. customthe solid precipitate removed by filtration
11. customthe filtrate was evaporated in vacuo
12. dissolutionThe residue was dissolved in hexane (50 mL)
13. customthe solid precipitate removed by filtration
14. customthe filtrate was evaporated in vacuo

ORDレコード

ord-d8db7c4b260e46d2adf106ecab333cbf

出典データセット

uspto-grants-2014_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08846696B2