Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843458Generated: October 30, 2026

Hydrochloric Acid → HCID 18755383, compound

https://huagongshe.com/reaction/843458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantSodium BicarbonateHCID 516892—
Reactant3,4-DifluoroanisoleHCID 568250—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
ProductHCID 18755383HCID 1875538392%

Reaction Conditions

Temperature60 °C

Reaction Steps

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376672B1
Source datasetuspto-grants-2002_04
ORD IDord-a0665c45bd9d4ffbb5f0a9fa1c07656a
Source noteuspto-grants-2002_04