HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900398Generated: October 30, 2026
Methylparaben → Methyl 4-[(quinolin-4-yl)methoxy]benzoate
https://huagongshe.com/reaction/900398
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylparaben | HCID 7456 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(Chloromethyl)quinoline | HCID 12355701 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Methyl 4-[(quinolin-4-yl)methoxy]benzoate | HCID 53689041 | — |
Reaction Steps
Sodium hydride (430 mg, 60%, 10.75 mmol) was placed in a flask with hexane and stirred under nitrogen. After 10 minutes the hexane was discarded and 10 ml dry DMF was added. After cooling to 0° C., 4-hydroxy-benzoic acid methyl ester Q-2 (1.67 g, 11 mmol) was added and the mixture stirred for 15 minutes. 4-Chloromethyl-quinoline Q-1 (1.8 g, 10.1 mmol) was dissolved in 3 mL of DMF and added dropwise to the reaction mixture. The temperature was raised to 130° C. and the mixture stirred for a half hour. After cooling to room temperature the reaction mixture was poured into 50 mL 1N sodium hydroxide solution and extracted three times with 20 mL dichloromethane. The combined organic layers were washed twice with water, dried over sodium sulfate and concentrated in vacuo. The crude product (2.5 g) was recrystallized from ethyl ether to give 4-(quinolin-4-ylmethoxy)-benzoic acid methyl ester (1.6 g, 5.45 mM) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07358373B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-ca819de813ae4c0681792a79e9720bd9 |
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| Source note | uspto-grants-2008_04 |
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