HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7331Generated: October 23, 2026
4-Hydroxybenzoic Acid → 4-(tetrahydro-2H-pyran-2-yloxy)benzoic acid
https://huagongshe.com/en/reaction/7331
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Hydroxybenzoic Acid | HCID 135 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Catalyst | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(tetrahydro-2H-pyran-2-yloxy)benzoic acid | HCID 11183645 | 86.2% |
Reaction Steps
Into a 300 ml three neck flask were charged 25.4 g of 2,3-dihydropyran (reagent, manufactured by Tokyo Kasei Kogyo Co., Ltd.), 41.4 g of p-hydroxybenzoic acid (reagent, manufactured by Tokyo Kasei Kogyo Co., Ltd.), and 3.7 g of pyridinium p-toluenesulfonate (reagent, manufactured by Tokyo Kasei Kogyo Co., Ltd.). The mixture was dissolved after addition of 20 ml of methylene chloride and 80 ml of absolute ether. After the mixture was vigorously stirred for about 3 hours, it was extracted 3 times with 70 ml of a 10% sodium hydroxide aqueous solution. The resulting extracted solution was neutralized with 1 N of hydrochloric acid until the pH is made to 6. The resulting precipitate was filtered and dried in a vacuum thereby obtaining 57.4 g of crude p-tetrahydropyranyloxy benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087273B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-1c09bba65c034d81b66bbb9495a49de8 |
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| Source note | uspto-grants-2006_08 |
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