Hydrochloric Acid → HCID 18755383, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5](OC)=[CH:4][C:3]=1[F:10].[CH2:11]=[O:12].[ClH:13].[C:14](=O)([O-])O.[Na+]>C(O)(=O)C.C(OCC)C>[Cl:13][CH2:5][C:6]1[CH:7]=[C:2]([F:1])[C:3]([F:10])=[CH:4][C:11]=1[O:12][CH3:14]Participants
Conditions
- Temperature
- 60 °C
Procedure
To a suspension of 5.75 g (40 mmol) of 1,2-difluoro-4-methoxy-benzene, 2.18 g (72 mmol) of paraformaldehyde and 3.55 g (25 mmol) of phosphorouspentoxide in 20 ml of acetic acid were added dropwise 7.2 ml of aqueous hydrochloric acid (37%). Thereupon, the reaction mixture was stirred for 18 hours at room temperature and additional 4 hours at 60° C. For the working up the mixture was hydrolyzed on crushed ice and 200 ml of diethylether were added. Under vigorous stirring 50 ml of saturated aqueous sodium hydrogencarbonate solution were added dropwise, then solid sodium hydrogencarbonate was added until the evolvement of carbondioxide had ceased. Subsequently, the organic phase was separated, extracted with saturated sodium chloride solution and dried over sodium sulfate. The solvent was evaporated and the crude product distilled. There were obtained 7.1 g (92% of theory) of 1-chloromethyl-4,5-difluoro-2-methoxy-benzene as a colorless liquid; b.p. ; 92-93° C. (6 Torr) ; MS: 192 (M)+.
Workup
- additionwere added
- additionwere added dropwise
- customSubsequently, the organic phase was separated
- extractionextracted with saturated sodium chloride solution
- dry with materialdried over sodium sulfate
- customThe solvent was evaporated
- distillationthe crude product distilled
Sources & evidence
- ORD record
- ord-cb4edfeac5014344a641d9d9a1af44a0
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06673931B2
Reaction notes
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