Water → HCID 46945306, compound

HRID 907511Notes

Reaction equation

HRID 907511 reaction equation
[S:1]([O:21][CH2:22][CH3:23])([O:3][CH2:4][C:5]([O:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])([O:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13])[CH3:6])=[O:2].[OH2:24]>CC#N.C(Cl)Cl>[S:1]([O:21][CH2:22][CH3:23])([O:3][CH2:4][C:5]([O:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])([O:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13])[CH3:6])(=[O:24])=[O:2]

Participants

5

Conditions

Temperature
23 °C

Procedure

To a solution of sulfite 6 (24.5 g, 69.5 mmol) in MeCN (200 mL), CH2Cl2 (200 mL) and water (300 mL) is added NaIO4 (29.7 g, 139.0 mmol) and RuCl3 (10 mg, 0.05 mmol). The mixture is stirred at 23° C. for 5 hours. The mixture is filtered through Celite and extracted with CH2Cl2 (2×200 mL). The combined organic layers are washed with saturated NaHCO3 (100 mL), brine (100 mL) and dried over anhydrous sodium sulfate. The solvent is removed and the residue is purified by silica gel chromatography (1→10% ethyl acetate/hexane) to give 2,2-bis(hexyloxy)propanyl ethyl sulfate 7 (23.3 g, 91%) as a colorless oil: Rf (15% EtOAc/hexane)=0.41; IR (thin film, cm−1) 2931, 2860, 1737, 1467, 1403, 1380, 1196, 1179, 1012, 925, 858; 1H NMR (600 MHz, CDCl3) δ 4.34 (q, J=7.2 Hz, 2H), 4.09 (s, 2H), 3.43 (ddd, J=9.0, 7.2, 6.6 Hz, 2H), 3.38 (ddd, J=9.0, 7.2, 6.6 Hz, 2H), 1.51 (m, 4H), 1.40 (t, J=7.2 Hz, 3H), 1.37 (s, 3H), 1.34-1.24 (m, 12H), 0.86 (t, J=7.2 Hz, 6H); 13C NMR (150 MHz, CDCl3) δ 98.2, 72.4, 69.7, 60.9, 31.6, 29.8, 25.9, 22.6, 20.8, 14.5, 14.0.

Workup

  1. filtrationThe mixture is filtered through Celite
  2. extractionextracted with CH2Cl2 (2×200 mL)
  3. washThe combined organic layers are washed with saturated NaHCO3 (100 mL), brine (100 mL)
  4. dry with materialdried over anhydrous sodium sulfate
  5. customThe solvent is removed
  6. customthe residue is purified by silica gel chromatography (1→10% ethyl acetate/hexane)

Sources & evidence

ORD record
ord-444240c1aab343ee95958c064f2a938c
Source dataset
uspto-grants-2011_09
Patent number
US08013179B2

Reaction notes

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