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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098211Generated: October 30, 2026

2-(Ethoxymethylene)propanedinitrile → HCID 57438663, compound

https://huagongshe.com/reaction/1098211

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Ethoxymethylene)propanedinitrileHCID 67152—
Reactant(5-Bromo-2-methylphenyl)hydrazine--hydrogen chloride (1/1)HCID 22279963—
SolventMethanolHCID 887—
ProductHCID 57438663HCID 5743866394%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143263B2
Source datasetuspto-grants-2012_03
ORD IDord-a2c3e0dc57ef42d9a890f6c31c1e685f
Source noteuspto-grants-2012_03