HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640754Generated: October 28, 2026
3-Chlorobenzaldehyde → Ethyl 3-(3-chlorophenyl)-2-propenoate
https://huagongshe.com/reaction/640754
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chlorobenzaldehyde | HCID 11477 | — |
| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester | HCID 70670 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-(3-chlorophenyl)-2-propenoate | HCID 367203 | 92% |
Reaction Steps
In a 2 l three necked flask fitted with mechanical stirrer and dropping funnel under inert atmosphere, 106.2 g (755 mmoles, 1 eq) of 3-chlorobenzaldehyde are dissolved in 1 l of THF and cooled down to 0° C. 341.9 g (980 mmoles, 1.3 eq) of ethyl (triphenylphosphoranylidene)acetate are then added under efficient stirring, the temperature raising to 10° C. The mixture is kept under stirring one hour at 0° C., and then overnight at room temperature. The mixture is concentrated to dryness, the residue suspended in diethyl ether, the triphenylphosphine oxide is filtered off and the filtrate concentrated to dryness. The residue is purified by PrepLC (1 kg SiO2, pet. ether/EtOAc, 75:35) to give 191.8 g of pure 375, 92% yield. 1H NMR (250 MHz, (CD3)2SO): 1.30 (t, 3H), 4.25 (q, 2H), 6.70 (d, 1H), 7.40 (m, 2H), 7.50-7.70 (m, 2H), 7.85 (s(broad), 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07692028B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-30ce98ebcfa14434bc531710a33548e6 |
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| Source note | uspto-grants-2010_04 |
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