HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654553Generated: October 31, 2026
Acetonitrile → 4-(6-Acryloyloxyhexyloxy)benzaldehyde
https://huagongshe.com/reaction/1654553
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | 4-(6-Hydroxyhexoxy)benzaldehyde | HCID 15051082 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(6-Acryloyloxyhexyloxy)benzaldehyde | HCID 19602217 | — |
Reaction Steps
8.9 g (0.04 mol) of 4-(6-hydroxyhexyloxy)benzaldehyde, 6.8 ml of triethylamine and 100 ml of acetonitrile were put in a three-neck flask equipped with a thermometer and a stirrer and cooled to 0° C. To this mixture was dropwise added a solution comprising 4.0 g (0.044 mol) of acryloyl chloride and 10 ml of acetonitrile with stirring at 0° C. to 5° C. After the addition, the whole mixture was stirred for one hour at 0° C. and poured into water containing ice. The crystals which precipitated out after a while were taken out by filtration, washed with water and dried by airing to obtain the intended compound. The yield of the product was 3.94 g (35.7%). The product had a melting point of 30° C. or lower.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05408009 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-c76380395ec44470a2b47e867b1373d6 |
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| Source note | uspto-grants-1995_04 |
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