HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098211Generated: October 30, 2026
2-(Ethoxymethylene)propanedinitrile → HCID 57438663, compound
https://huagongshe.com/reaction/1098211
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Ethoxymethylene)propanedinitrile | HCID 67152 | — |
| Reactant | (5-Bromo-2-methylphenyl)hydrazine--hydrogen chloride (1/1) | HCID 22279963 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57438663 | HCID 57438663 | 94% |
Reaction Steps
5 (5-Bromo-2-methylphenyl)hydrazine hydrochloride (CAS no. 214915-80-7) (5 g, 21.05 mmol) was partitioned between EtOAc (50 mL) and NaOH (2M, aq) (30 mL). The organic layer separated and washed with water (50 mL), brine (50 mL), dried (MgSO4), filtered and concentrated to afford free base of the starting material. The resultant oil was suspended in MeOH (50 mL) under nitrogen at −5° C. 2-(ethoxymethylene)malononitrile (2.57 g, 21.05 mmol) added portionwise over 5 mins and the mixture stirred at ˜0° C. for 30 mins. The reaction mixture was allowed to warm to room temperature and then heated at reflux under nitrogen for 2 hours. The reaction mixture was allowed to cool and evaporated to dryness to afford the product (5.48 g, 94%). 1H NMR (400 MHz, DMSO) 1.99 (3H, s), 6.59 (2H, s), 7.36 (1H, d), 7.49 (1H, d), 7.60-7.63 (1H, m), 7.76 (1H, s); m/z (ES+) (M+H)+=277+279; HPLC tR=2.01 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143263B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-a2c3e0dc57ef42d9a890f6c31c1e685f |
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| Source note | uspto-grants-2012_03 |
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