Dimethyl Sulfoxide → (S)-2-Dibenzylamino-propionaldehyde

Dry DMSO (0.53 ml, 7.43 mmol) was added to a stirred solution of oxalyl chloride (0.31 ml, 3.6 mmol) in CH2Cl2 (7.5 ml) at −78° C. The solution was allowed to stir 15 minutes followed by the addition of 40 (740 mg, 2.90 mmol) in CH2Cl2 (7.5 ml). After 30 minutes, Et3N (1.0 ml, 7.2 mmol) was added and allowed to warm to room temperature. The solution was extracted with saturated. NaHCO3 (20 ml) and the aqueous layer was extracted with CH2Cl2 (2×15 ml). The organic layer was washed with saturated. NaCl solution, dried with MgSO4 an concentrated in vacuo at room temperature to give 720 mg (98% yield) of a yellow oil which became a solid when cooled to −20° C. The aldehyde was used without further purification: mp 52–54° C., Literature mp 55.5° C. See, Dix et al., Arch Pharm (Weinheim) 1995, 328, 203–205.; [α]26D=−36.0 (c 1, CHCl3) Literature [α]20D=−35.1 (c 1, EtOAc); 1H NMR (400 MHz, CDCl3) d 1.19 (d, 2H, J=7.0 Hz), 3.34 (q, 1H, J=7.0 Hz), 3.58 (δ, 2H, J=13.7 Hz), 3.74 (d, 2H, J=13.7 Hz), 7.26 (m, 2H), 7.33 (m, H), 7.42 (m, 4H), 9.74 (s, 1H); 13C NMR (100 MHz) δ 6.7, 54.9, 62.8, 3.3, 4.4, 4.8, 139.1, 204.6; FABMS m/z 408.2 (M+MB), 254.2 (M+H), 22.2 (M-CHO); HRFABMS calcd for C17H20NO Mr 254.1545 (M+H), found Mr 254.1545.

1. waitAfter 30 minutes
2. extractionThe solution was extracted with saturated
3. extractionNaHCO3 (20 ml) and the aqueous layer was extracted with CH2Cl2 (2×15 ml)
4. washThe organic layer was washed with saturated
5. dry with materialNaCl solution, dried with MgSO4
6. concentrationan concentrated in vacuo at room temperature

ORD record

ord-92ae5657dd784c9ca7c0362503f68d87

Source dataset

uspto-grants-2006_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07109244B2