N,N-Dimethylaniline → HCID 15671658, compound
Reaction equation
[Br:1][CH2:2][C:3](Br)=[O:4].[Cl:6][C:7](=[CH2:10])[CH2:8][OH:9].CN(C)C1C=CC=CC=1>ClCCl>[Br:1][CH2:2][C:3]([O:9][CH2:8][C:7]([Cl:6])=[CH2:10])=[O:4]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 23 °C
Procedure
To a cold (0° C.) solution of bromoacetyl bromide (51.5 g, 25.5 mmol) in dichloromethane (80 mL) kept under nitrogen atmosphere was added 2-chloroallyl alcohol (26.0 g, 28.1 mmol) over 5 minutes period and N,N-dimethylaniline (30.9 g, 25.5 mmol) at such a rate that the temperature was kept below 5° C. (30 minutes). When the addition was completed, the cooling bath was removed and, the mixture was stirred for 2 hours at 23° C. and washed with water (25 mL), 0.1N HCl (2×25 mL) and water (25 mL). The organic solution was dried (Na2SO4) and concentrated to a crude material from which the title compound was distilled; 44.8 g, 82%, bp 74°-6° C./1.25 torr; ir (neat) νmax : 1745 (C=O), 1635 (C=C) cm-1 ; 1Hmr (CDCl3) δ: 3.93 (s, BrCH2), 4.73 (s, COOCH2C(Cl)=C2), 5.48 (m, COOCH2C(Cl)=CH2). Anal. calcd. for C5H6O2BrCl: C 28.13, H 2.83, Cl 16.61; found: C 28.49, H 2.92, Cl 16.78
Workup
- customwas kept below 5° C.
- custom(30 minutes)
- additionWhen the addition
- customthe cooling bath was removed
- washwashed with water (25 mL), 0.1N HCl (2×25 mL) and water (25 mL)
- dry with materialThe organic solution was dried (Na2SO4)
- concentrationconcentrated to a crude material from which the title compound
- distillationwas distilled
Sources & evidence
- ORD record
- ord-16cf8b1dd63c40df8c63b9cd8438d435
- Source dataset
- uspto-grants-1988_09
- Patent number
- US04769451
Reaction notes
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