HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429863Generated: October 31, 2026
Acetic Acid → methyl [(4E)-1-(2-chlorophenyl)-4-(1-ethoxyethylidene)-5-oxo-4,5-dihydro-1H-pyrazol-3-yl]acetate
https://huagongshe.com/reaction/1429863
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Triethyl orthoacetate | HCID 66221 | — |
| Reactant | HCID 178499531 | HCID 178499531 | — |
| Product | methyl [(4E)-1-(2-chlorophenyl)-4-(1-ethoxyethylidene)-5-oxo-4,5-dihydro-1H-pyrazol-3-yl]acetate | HCID 86701218 | — |
Reaction Steps
The mixture of the above obtained methyl[1-(2-chlorophenyl)-5-hydroxy-1H-pyrazol-3-yl]acetate (Compound of Formula (IV), 1.00 g), glacial acetic acid (21 μl, 0.1 equiv.) and MeC(OEt)3 (2.00 ml) was heated at 60° C. for 1 h 15. The resulting red solution was concentrated in vacuo to afford a red syrup that was washed with cyclohexane and then dried in vacuo. Due to its relative instability, no further purification of methyl[(4E)-1-(2-chlorophenyl)-4-(1-ethoxyethylidene)-5-oxo-4,5-dihydro-1H-pyrazol-3-yl]acetate was conducted (1.26 g, quantitative yield). MS (ESI+): 336.8; MS (ESI−): 334.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940760B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-c39b2f41d6274e998be89189a08ecbb4 |
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| Source note | uspto-grants-2015_01 |
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