HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223995Generated: October 31, 2026
N,N-Dimethylaniline → (4-(6-Acryloyloxyhexyloxy)phenyl)propionic acid
https://huagongshe.com/reaction/2223995
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | (4-(6-Hydroxyhexyloxy)phenyl)propionic acid | HCID 67067011 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (4-(6-Acryloyloxyhexyloxy)phenyl)propionic acid | HCID 67067021 | 88.5% |
Reaction Steps
(4-(6-Hydroxyhexyloxy)phenyl)propionic acid (200 g), N,N-dimethylaniline (100 g) and BHT (0.3 g) were dissolved in dioxane (1,000 mL). Acrylic acid chloride (74.3 g) was added dropwise thereto over 10 minutes, followed by agitating at 60° C. for 5 hours. The reaction solution was poured into water, to which ethyl acetate was added, followed by agitating. The ethyl acetate layer was separated, washed with water, and then dried over anhydrous magnesium sulfate. The solvent was distilled off from the ethyl acetate layer to obtain a solid product. The solid product was dissolved in toluene and reprecipitated by pouring into a large amount of heptane to obtain 213 g of (4-(6-acryloyloxyhexyloxy)phenyl)propionic acid. (Melting point: 64 to 68° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07378135B2 |
|---|
| Source dataset | uspto-grants-2008_05 |
|---|
| ORD ID | ord-0052e64c7fd14160996ec32c1c2a1f68 |
|---|
| Source note | uspto-grants-2008_05 |
|---|