Diethyl Ether → HCID 19432448, compound

HRID 2209838Notes

Reaction equation

HRID 2209838 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[C:9]3[CH:10]=[CH:11][C:12]([CH2:14][OH:15])=[CH:13][C:8]=3[O:7][C:6]=2[CH:16]=1.[Si:17](Cl)([C:20]([CH3:23])([CH3:22])[CH3:21])([CH3:19])[CH3:18].C(N(CC)CC)C.C(OCC)C>C1COCC1.CN(C)C1C=CN=CC=1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[C:9]3[CH:10]=[CH:11][C:12]([CH2:14][O:15][Si:17]([C:20]([CH3:23])([CH3:22])[CH3:21])([CH3:19])[CH3:18])=[CH:13][C:8]=3[O:7][C:6]=2[CH:16]=1

Participants

7

Reactant 4

HCID 3283Diethyl EtherHCID 8471TriethylamineHCID 28928tert-Butyldimethylsilyl chlorideHCID 19432446HCID 19432446, compound

Product 1

HCID 19432448HCID 19432448, compoundYield 82.6%

Reagents, catalysts & solvents 2

HCID 142844-(Dimethylamino)pyridineCatalystHCID 8028TetrahydrofuranSolvent

Procedure

To a solution of 3-bromo-7-hydroxymethyldibenzofuran (2.74 g, 9.9 mmol) and t-butyldimethylsilyl chloride (1.93 g, 12.8 mmol) in THF (60 ml) was added triethylamine (1.95 ml, 13.8 mmol) followed by 4-dimethylaminopyridine (DMAP) (120.7 mg, 0.99 mmol). After stirring at room temperature for 20 hours, the solution was poured into ethyl ether (180 ml) and washed successively with saturated NH4Cl, saturated NaHCO3, H2O and brine. Drying (MgSO4) and evaporation gave a brown solid which was purified by flash chromatoraphy through 100 g silica gel (10% CH2Cl12 hexane) to yield 3.2 g (82%) of the title compound as a pale yellow solid.

Workup

  1. washwashed successively with saturated NH4Cl, saturated NaHCO3, H2O and brine
  2. customDrying
  3. custom(MgSO4) and evaporation
  4. customgave a brown solid which
  5. customwas purified by flash chromatoraphy through 100 g silica gel (10% CH2Cl12 hexane)

Sources & evidence

ORD record
ord-0df84d66f44b4c75b8c3e8edc764591f
Source dataset
uspto-grants-1995_10
Patent number
US05455239

Reaction notes

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