HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730256Generated: October 29, 2026
Aniline → (E)-3-(4-tert-Butyl-phenyl)-N-phenyl-acrylamide
https://huagongshe.com/reaction/730256
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-(Tert-butyl)cinnamic acid | HCID 724839 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (E)-3-(4-tert-Butyl-phenyl)-N-phenyl-acrylamide | HCID 5885566 | — |
Reaction Steps
To a 10 mL glass vial was added 4-tert-butyl-trans-cinnamic acid (200 mg, 0.98 mmol, EMKA-Chemie) followed by CH2Cl2 (5 mL), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (225 mg, 1.17 mmol, Bachem) and aniline (98 uL, 100 mg, 1.08 mmol, Aldrich). The reaction mixture was magnetically stirred at 25° C. for 24 h. EtOAc was added (60 mL) and the mixture washed successively with 1 N NaOH (2×20 mL), 1 N HCl (20 mL), water (20 mL) and satd NaCl (20 mL), dried over MgSO4, filtered and concentrated. Recrystallization from hexane and CH2Cl2 provided the title product as white crystals. MP 141° C. MS (ESI, pos. ion) m/z: 280 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582657B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-0da29454cdb04e7698bda38a4d2fc137 |
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| Source note | uspto-grants-2009_09 |
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