HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187948Generated: October 30, 2026
Hydrochloric Acid → 4-Bromo-alpha-chloro-3-methylbenzaldoxime
https://huagongshe.com/reaction/1187948
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | 4-Bromo-3-methylbenzaldehyde oxime | HCID 73847954 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Bromo-alpha-chloro-3-methylbenzaldoxime | HCID 86611478 | 98.2% |
Reaction Steps
In a solution of 82.0 g of 4-bromo-3-methylbenzaldoxime in 450 mL of tetrahydrofuran, 120.0 g of concentrated hydrochloric acid was added dropwise under cooling with ice and with stirring over 45 minutes. Then, 220 mL of 8% sodium hypochlorite aqueous solution was added dropwise over 75 minutes carefully so that the temperature of the reaction mixture would not exceed 5° C. After the completion of the addition dropwise, it was continued to stir at a temperature of 10° C. or less for further 90 minutes. After the completion of the reaction, the reaction mixture was blown with nitrogen gas for 45 minutes, then precipitated insoluble material was filtered off, tetrahydrofuran was distilled off under reduced pressure. The residual aqueous solution was extracted with 240.0 g of ethyl acetate, and the organic phase was washed with water (240 mL×2). The insoluble material was filtered off, the solvent was distilled off under reduced pressure to obtain 93.5 g of the aimed product as pale yellow crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673951B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-fa7317e1e0b44494b2abc7e2c5b6c258 |
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| Source note | uspto-grants-2014_03 |
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