HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623637Generated: October 30, 2026
5-Bromosalicylic acid → HCID 67107142, compound
https://huagongshe.com/reaction/1623637
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Bromosalicylic acid | HCID 6972 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methoxybenzyl bromide | HCID 165021 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 67107142 | HCID 67107142 | — |
Reaction Steps
1-(Bromomethyl)-4-methoxybenzene (510 mg, 2.53 mmol) was added in a single charge to a stirred suspension of 5-bromo-2-hydroxybenzoic acid (250 mg, 1.15 mmol) and potassium carbonate (318 mg, 2.30 mmol) in acetone (40 ml) over 1 min under nitrogen. The reaction mixture was stirred at 55° C. for 16 h. The organic phase was evaporated and the residue was washed with water (25 ml), extracted with ethyl acetate (3×30 ml) and evaporated in vacuo to yield the title compound as a light yellow solid. 400 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778939B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-d96f3ed5948a45db86e7db2ece442129 |
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| Source note | uspto-grants-2014_07 |
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