HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382829Generated: October 28, 2026
Bromine → 2,4-Bis(acetoxymethyl)bromobenzene
https://huagongshe.com/reaction/382829
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | m-Xylylene glycol diacetate | HCID 12571717 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2,4-Bis(acetoxymethyl)bromobenzene | HCID 9948291 | 97.7% |
Reaction Steps
To a suspension of m-xylylene glycol diacetate (28.4 g) and sodium acetate (55.2 g) dispersed in glacial acetic acid (130 ml) was added dropwise bromine (102.5 g) over 30 min at 15-20° C., and the mixture was stirred at 20-30° C. for 13 hr. The reaction mixture was poured into 10% aqueous sodium sulfite solution (700 ml) in an ice bath. The mixture was stirred and extracted twice with ethyl acetate (250 ml). The ethyl acetate layer was washed 3 times with 10% aqueous sodium hydrogencarbonate solution (300 ml) and the solvent was evaporated to give an about 93:7 mixture (37.6 g, 97.6%) of 2,4-bis(acetoxymethyl)bromobenzene and 2,6-bis(acetoxymethyl)bromobenzene as a yellow oil. 2,4-bis(Acetoxymethyl)bromobenzene was isolated by preparative HPLC and used in the measurement.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310222B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-77b36ee54f4c4f05bd0f4218595e7fc7 |
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| Source note | uspto-grants-2001_10 |
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