Pyridine → HCID 85218918, compound

HRID 1817668Notes

Reaction equation

HRID 1817668 reaction equation
[O:1]([CH:19]([CH3:24])[CH2:20][CH2:21][CH2:22][OH:23])[Si:2]([C:15]([CH3:18])([CH3:17])[CH3:16])([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.N1C=CC=CC=1.[S:31](Cl)([C:34]1[CH:40]=[CH:39][C:37]([CH3:38])=[CH:36][CH:35]=1)(=[O:33])=[O:32]>C(Cl)Cl>[O:1]([CH:19]([CH3:24])[CH2:20][CH2:21][CH2:22][O:23][S:31]([C:34]1[CH:40]=[CH:39][C:37]([CH3:38])=[CH:36][CH:35]=1)(=[O:33])=[O:32])[Si:2]([C:15]([CH3:16])([CH3:17])[CH3:18])([C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

Participants

5

Procedure

4-(t-Butyldiphenylsiloxy)-pentanol (15 g, 0.04 mol) was dissolved in methylene chloride (100 mL) containing pyridine (7 g). Tosyl chloride (15.3 g, 0.08 mol) was added slowly and the mixture stirred overnight. The mixture was washed with saturated NaHCO3 (2×100 mL) and the aqueous then backwashed with methylene chloride (100 mL). The organic phases were combined and washed with 2M HCl (100 mL) and water. The solution was dried over Na2SO4, evaporated and purified by column chromatography (light petroleum: ethyl acetate, 3:1) to give the title compound as a thick oil (yield 85%). δC (CDCl3, 62.9 MHz): 19.2, 21.7, 21.8, 26.9, 28.6, 31.8, 63.5, 70.6, 127.7, 127.9, 129.6, 129.9, 133.2, 133.9, 135.6 and 144.7

Workup

  1. washThe mixture was washed with saturated NaHCO3 (2×100 mL)
  2. washwashed with 2M HCl (100 mL) and water
  3. dry with materialThe solution was dried over Na2SO4
  4. customevaporated
  5. custompurified by column chromatography (light petroleum: ethyl acetate, 3:1)

Sources & evidence

ORD record
ord-d535c5917c304f6a809382415a8c8b9f
Source dataset
uspto-grants-2009_10
Patent number
US07598289B2

Reaction notes

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