Diisobutylaluminumhydride → 476198-98-8

HRID 2220304Notes

Reaction equation

HRID 2220304 reaction equation
[F:1][C:2]1[C:10]2[S:9][C:8](=O)[CH2:7][C:6]=2[C:5]([O:12][CH3:13])=[CH:4][CH:3]=1.[H-].C([Al+]CC(C)C)C(C)C>ClCCl>[F:1][C:2]1[C:10]2[S:9][CH:8]=[CH:7][C:6]=2[C:5]([O:12][CH3:13])=[CH:4][CH:3]=1

Participants

4

Conditions

Temperature
35 °C

Procedure

To a solution of 7-fluoro-4-methoxy-1-benzothiophen-2(3H)-one (1.06, 5.4 mmol) in dichloromethane (10 mL) at 0° C. was added slowly a solution of diisobutylaluminium hydride in dichloromethane (1 M, 8.04 mL, 8.0 mmol). After 30 mins the reaction was quenched by careful addition of aqueous hydrochloric acid (6 N, 25 mL). The mixture was concentrated to remove the dichloromethane, the aqueous residue was then stirred at 35° C. for 2 h. The aqueous solution was extracted with diethyl ether (3×50 mL), washed with aqueous sodium hydroxide (2 N, 50 mL), brine (50 mL) then dried (MgSO4) and the solvent evaporated in vacuo to give the title compound (0.86 g, 87%) as a purple oil; δH 7.44-7.38 (1H, m, ArH), 7.36-7.24 (1H, m, ArH), 6.88-6.80 (1H, m, ArH), 6.57-6.49 (1H, m, ArH) and 3.82 (3H, s, OCH3).

Workup

  1. customAfter 30 mins the reaction was quenched by careful addition of aqueous hydrochloric acid (6 N, 25 mL)
  2. concentrationThe mixture was concentrated
  3. customto remove the dichloromethane
  4. extractionThe aqueous solution was extracted with diethyl ether (3×50 mL)
  5. washwashed with aqueous sodium hydroxide (2 N, 50 mL), brine (50 mL)
  6. dry with materialthen dried (MgSO4)
  7. customthe solvent evaporated in vacuo

Sources & evidence

ORD record
ord-7bf3b3cd5781498a9af258dfc5d68e90
Source dataset
uspto-grants-2008_08
Patent number
US07417064B2

Reaction notes

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