Triethylamine → 950785-37-2

HRID 1988628Notes

Reaction equation

HRID 1988628 reaction equation
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][NH2:7])=[CH:4][CH:3]=1.C(N(CC)CC)C.Cl[CH2:18][CH2:19][CH2:20][S:21](Cl)(=[O:23])=[O:22].[H-].[Na+]>CN(C)C=O>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][N:7]2[CH2:18][CH2:19][CH2:20][S:21]2(=[O:23])=[O:22])=[CH:4][CH:3]=1

Participants

6

Procedure

A solution of 4-bromobenzylamine (1.85 g, 10 mmol) and triethylamine (2 g, 20 mmol) in dimethylformamide (30 ml) was treated with 3-chloropropanesulfonyl chloride (1.78 g, 10 mmol) by dropwise addition over 10 minutes with stirring under argon. This mix was stirred for 30 minutes before being treated with a 60% suspension of sodium hydride in mineral oil (1.2 g, 30 mmol of NaH) portionwise and the whole mix stirred at room temperature for 3 days. The reaction mixture was partitioned between water (50 ml) and dichloromethane (30 ml). The organic layer was dried over sodium sulphate and reduced to minimum volume by rotary evaporation. The residue was added to a 20 g pre-packed silica column and eluted from 0-50% ethyl acetate in petroleum ether to give the title compound as a yellow oil (2.72 g, 94%).

Workup

  1. stirringThis mix was stirred for 30 minutes
  2. additionthe whole mix
  3. stirringstirred at room temperature for 3 days
  4. customThe reaction mixture was partitioned between water (50 ml) and dichloromethane (30 ml)
  5. dry with materialThe organic layer was dried over sodium sulphate
  6. customreduced to minimum volume by rotary evaporation
  7. additionThe residue was added to a 20 g pre-packed silica column
  8. washeluted from 0-50% ethyl acetate in petroleum ether

Sources & evidence

ORD record
ord-fc7c0eecd520456cacbb1ee0086daca7
Source dataset
uspto-grants-2010_01
Patent number
US07642256B2

Reaction notes

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