2-Chloro-N-methoxy-N-methylacetamide → HCID 22473705, compound

HRID 2183629Notes

Reaction equation

HRID 2183629 reaction equation
Br[C:2]1[C:3]2[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:4]=2[S:5][CH:6]=1.C([Li])CCC.[Cl:17][CH2:18][C:19](N(OC)C)=[O:20]>O1CCCC1.CCOCC>[Cl:17][CH2:18][C:19]([C:6]1[S:5][C:4]2[CH:7]=[CH:8][CH:9]=[C:10]([CH3:11])[C:3]=2[CH:2]=1)=[O:20]

Participants

6

Conditions

Temperature
-70 °C

Procedure

A solution of 3-bromo-4-methylbenzo[b]thiophene (2 g) in tetrahydrofuran (10 ml) was added dropwise under nitrogen at −70° C. over 10 minutes to a stirred solution of n-butyllithium (2.5M solution in hexanes; 4.58 ml) in ether (30 ml), then the mixture was stirred at −70° C. for 30 minutes. A solution of 2-chloro-N-methoxy-N-methylacetamide (1.04 g) in tetrahydrofuran (10 ml) was added dropwise at −70° C. over 10 minutes, then the mixture was stirred at −70° C. for 5 hours, allowed to stand at ambient temperature for 18 hours and quenched by the addition of saturated aqueous ammonium chloride solution (40 ml). The organic layer was separated, washed with saturated aqueous sodium chloride solution (40 ml), and dried (MgSO4). The solvents were removed in vacuo to give 2-chloro-1-(4-methylbenzo[b]thiophen-2-yl]ethan-1-one (1.65 g) as a brown oil which was used without further purification.

Workup

  1. stirringthe mixture was stirred at −70° C. for 5 hours
  2. waitto stand at ambient temperature for 18 hours
  3. customquenched by the addition of saturated aqueous ammonium chloride solution (40 ml)
  4. customThe organic layer was separated
  5. washwashed with saturated aqueous sodium chloride solution (40 ml)
  6. dry with materialdried (MgSO4)
  7. customThe solvents were removed in vacuo

Sources & evidence

ORD record
ord-16932680358547ec8d79f0ca05a7577f
Source dataset
uspto-grants-2005_05
Patent number
US06900216B2

Reaction notes

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