Water → 5-Bromo-4-chloro-2-methoxymethoxybenzyl cyanide

HRID 862072Notes

Reaction equation

HRID 862072 reaction equation
[Br:1][C:2]1[C:3]([Cl:14])=[CH:4][C:5]([O:10][CH2:11][O:12][CH3:13])=[C:6]([CH:9]=1)[CH2:7]O.[CH2:15]([N:17](CC)CC)C.CS(Cl)(=O)=O.O>ClCCl>[Br:1][C:2]1[C:3]([Cl:14])=[CH:4][C:5]([O:10][CH2:11][O:12][CH3:13])=[C:6]([CH:9]=1)[CH2:7][C:15]#[N:17]

Participants

6

Procedure

To a solution of 5-bromo-4-chloro-2-methoxymethoxybenzyl alcohol (137.9 g) and triethylamine (105 ml) in dichloromethane (500 ml) was added at 0° C. methanesulfonyl chloride (45.5 ml) over a period of 30 minutes. The mixture was stirred overnight (13 hours), while warming up to room temperature. The reaction mixture was poured into water, to which was added dichloromethane for extraction. The extract solution was dried (anhydrous magnesium sulfate) and concentrated. To a suspension of the concentrate and sodium cyanide (51.4 g) in dichloromethane (40 ml) was added dropwise at 0° C. DMSO (300 ml). The mixture was then stirred for 3 hours at room temperature. The reaction mixture was poured into water, which was subjected to extraction with ethyl acetate. The extract solution was washed with water, dried (anhydrous magnesium sulfate) and concentrated. The concentrate was purified by means of a silica gel column chromatography (eluted with ethyl acetate/hexane) to give 5-bromo-4-chloro-2-methoxymethoxybenzyl cyanide (86.4 g) (Compound B-35). The physical properties are shown in [Table 6].

Workup

  1. extractionfor extraction
  2. dry with materialThe extract solution was dried (anhydrous magnesium sulfate)
  3. concentrationconcentrated
  4. additionTo a suspension of the
  5. concentrationconcentrate
  6. additionsodium cyanide (51.4 g) in dichloromethane (40 ml) was added dropwise at 0° C
  7. stirringThe mixture was then stirred for 3 hours at room temperature
  8. additionThe reaction mixture was poured into water, which
  9. extractionwas subjected to extraction with ethyl acetate
  10. washThe extract solution was washed with water
  11. dry with materialdried (anhydrous magnesium sulfate)
  12. concentrationconcentrated
  13. customThe concentrate was purified by means of a silica gel column chromatography (eluted with ethyl acetate/hexane)

Sources & evidence

ORD record
ord-7d98c758b67442c79ad3cadb8fb5f9d7
Source dataset
uspto-grants-1998_02
Patent number
US05716971

Reaction notes

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