HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374857Generated: October 31, 2026
Ethyl cyanoacetate → Ethyl 2-ethoxyethylidene-cyanoacetate
https://huagongshe.com/reaction/1374857
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Triethyl orthoacetate | HCID 66221 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Product | Ethyl 2-ethoxyethylidene-cyanoacetate | HCID 57299996 | 82.6% |
Reaction Steps
To a stirred solution of Ethyl cyanoacetate (46.8 g, 414 mMol) and Triethyl orthoacetate (84.4 g, 520 mMol), in a 250 mL round bottom flask fitted with a short path distillation head, was added HOAc (1.2 mL, 21 mMol). The reaction was slowly heated to 135° C. and maintained at that temperature to distill off the ethyl alcohol that was produced. (Distillation started at ˜106° C.) At 15 min. intervals HOAc (1.2 mL, 21 mMol) was added to the reaction for an additional three times. The reaction was then slowly heated to 150° C. then cooled back down to ˜80° C. The title product (62.64 g, 82%) was obtained by short path distillation under high vacuum (bp 128° C., HV) as a pale yellow crystalline solid. (Note; Cooling to the condenser was shut off to prevent plugging.): 1H NMR (400 MHz, CDCl3) δ 4.27 (q, 2H), 4.22 (q, 2H), 2.61 (s, 3H), 1.43 (t, 3H), 1.31 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07166595B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-7db0819026ee433b952c5a9805deda49 |
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| Source note | uspto-grants-2007_01 |
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