HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223994Generated: October 31, 2026
N,N-Dimethylaniline → HCID 69250913, compound
https://huagongshe.com/reaction/2223994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | HCID 69251770 | HCID 69251770 | — |
| Catalyst | 2,6-Dibutyl-4-methylphenol | HCID 11117575 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69250913 | HCID 69250913 | — |
Reaction Steps
Under a nitrogen atmosphere, 4-(6-hydroxyhexyloxy)-2-fluorobenzoic acid (189 g), N,N-dimethylaniline (133 g) and 2,6-dibutyl-p-cresol (0.80 g) were added to tetrahydrofuran (500 mL). Acrylic acid chloride (100 g) was added dropwise thereto, followed by agitating at 60° C. for 3 hours. The reaction solution was poured into water and extracted with ethyl acetate. The organic layer was washed with hydrochloric acid, a saturated sodium hydrogencarbonate aqueous solution and water, and after drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was recrystallized from ethanol to obtain 4-(6-acryloylhexyloxyhexyloxy)-2-fluorobenzoic acid (141 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07378135B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-ca72d716246f4bfab9b90c9e30af08c1 |
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| Source note | uspto-grants-2008_05 |
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