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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983844Generated: November 3, 2026

Hydrochloric Acid → HCID 23031791, compound

https://huagongshe.com/reaction/1983844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzoyl chloride, 3-bromo-HCID 74377—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-Chloro-4-methoxytolueneHCID 6951757—
SolventChlorobenzeneHCID 7964—
SolventTetrahydrofuran tolueneHCID 22635083—
ProductHCID 23031791HCID 2303179185.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

Aluminum chloride (20.4 g) was added to a solution of 3-chloro-4-methylanisole (20 g) in chlorobenzene (56 ml) at 20-30° C., and then 3-bromobenzoyl chloride (28 g) was further added dropwise over about 30 minutes at 25 to 30° C. After completion of addition, the mixture was stirred at 25° C. for 1 hour, and then heated at 40° C. for 1 hour. After the reaction was completed, the mixture was cooled, and toluene/tetrahydrofuran (1:1, 200 ml) was added dropwise at 20 to 30° C. Then, 4N hydrochloric acid (80 ml) was added dropwise. The organic layer was separated, washed successively with 2N hydrochloric acid (60 ml) and a 10% aqueous sodium chloride solution. The organic layer was concentrated to 80 g. After methanol (100 ml) was added, the mixture was concentrated again to 90 g. Methanol (80 ml) was added to the residue, the mixture was stirred at room temperature for 30 minutes, and below 5° C. for 1 hour. Crystals were collected, washed with cooled methanol (40 ml) and dried under reduced pressure to obtain the title compound (35.4 g, yield 85.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541478B2
Source datasetuspto-grants-2009_06
ORD IDord-3247996006d74cdeb926b65fa7387bb1
Source noteuspto-grants-2009_06