HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189710Generated: October 29, 2026
Acetic Acid → 2-Naphthalenecarboxylic acid, 7-bromo-3-hydroxy-
https://huagongshe.com/reaction/1189710
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy- | HCID 74502 | — |
| Reactant | Tin atom | HCID 5352426 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Naphthalenecarboxylic acid, 7-bromo-3-hydroxy- | HCID 74503 | 96.5% |
Reaction Steps
In a 1 L three-necked bottle, 40 g of 4,7-dibromo-3-hydroxy-2-naphthoic acid (0.116 mol) and 500 ml of glacial acetic acid were added, and stirred to make homogenous. 18 g of tin powder (0.153 mol) and 130 ml of concentrated hydrochloric acid were then added to the mixture in order, heated to 125° C., and refluxed under heating for 12 h. 300 ml of water was added to the mixture, stirred to room temperature, filtered, and the filter cake was washed with water (200 ml*2), and dried in an oven to obtain 29.9 g of a solid with a yield of 96.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08674136B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-dc5fa820f87644598b971facd31ebc4a |
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| Source note | uspto-grants-2014_03 |
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