HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712171Generated: November 3, 2026
Acrylonitrile → 3-(4-Methoxyphenoxy)propanenitrile
https://huagongshe.com/reaction/1712171
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Product | 3-(4-Methoxyphenoxy)propanenitrile | HCID 114247 | 76.9% |
Reaction Steps
4-Methoxyphenol (263.0 g) was dissolved in acrylonitrile (224.8 g), and then Triton B (18 mL) was added dropwise at room temperature, with stirring at 80° C. for 48 hours. The reaction liquor was returned to room temperature while slowly stirring, and stirred for 12 hours. The reaction liquor was further left to stand at 6° C. to precipitate white prisms. The mother liquor was subjected to decantation, and cold toluene (300 mL) was added to obtain crystals, and then the resulting crude crystals were dried at room temperature under reduced pressure (3 hours) (crude crystals 232.6 g). The crude crystals were dissolved in ethyl acetate (250 mL) at 50° C., n-heptane (250 mL) was slowly added with stirring, and the resulting mixture was recrystallized with slow stirring for 12 hours. The mother liquor was subjected to decantation, n-heptane (300 mL) was added, and crystals were obtained. The crystals were washed with n-heptane (400 mL) and dried at room temperature under reduced pressure (crystal No. 1: white prisms 154.5 g). Since crystals were generated in the mother liquor, pale yellow prisms were obtained as crystal No. 2 (crystal No. 2: pale yellow prisms 56.1 g). All of the filtrate and n-heptane used for washing were recovered and concentrated under reduced pressure. Then, toluene (500 mL) was added to the residue, and the mixture was washed with 1 N aqueous sodium hydroxide solution (100 mL×3 times), water (500 mL), 1 N aqueous hydrochloric acid solution (100 mL×3 times), water (500 mL) and saturated brine (300 mL), then dried over anhydrous sodium sulfate for 30 minutes, and filtered, and subsequently the filtrate was concentrated under reduced. The residue was dissolved in ethyl acetate (150 mL) at 50° C., and n-heptane (150 mL) was slowly added with stirring, and the resulting mixture was recrystallized with slow stirring for 12 hours. The mother liquor was subjected to decantation, and n-heptane (200 mL) was added, and crystals were obtained. The crystals were washed with n-heptane (300 mL) and dried at room temperature under reduced pressure (crystal No. 3: white prisms 59.0 g). Furthermore, pale yellow prisms were obtained as crystal No. 4 (crystal No. 4: 19.0 g). Total amount obtained was 288.6 g, yield was 76.9%+ crude crystals (yellow prisms, 21.8 g, 5.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790903B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-6197b9ff6b3c4066b99cae45895cae36 |
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| Source note | uspto-grants-2010_09 |
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