HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243646Generated: October 29, 2026
3-Chlorobenzaldehyde → HCID 14185029, compound
https://huagongshe.com/reaction/243646
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chlorobenzaldehyde | HCID 11477 | — |
| Reactant | HCID 178461836 | HCID 178461836 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14185029 | HCID 14185029 | 44% |
Reaction Steps
To a cooled solution of 3-chlorobenzaldehyde (22.5 g, 160 mmol) in 100 mL anhydrous THF under inert nitrogen atmosphere was added slowly via syringe a 1.6 M solution of vinyl magnesium chloride in THF (100 mL, 160 mmol) and the solution stirred for three h allowing to warm to room temperature. The reaction was quenched with saturated solution of ammonium chloride and the organic layer was separated, extracted with ethyl acetate (2×200 mL), and organic layers were combined, dried over magnesium sulfate, filtered and concentrated under vacuum. Purification by Horizon MPLC with a 40M+ silica gel column using a gradient eluent of 0-40% ethyl acetate in hexane afforded the title compound (22.4 g, 44%). m/z (ES) 168, 170 (M, M+2)+, 190, 192 (MNa, MNa+2)+. 1HNMR (500 MHz, CDCl3) δ: 7.38 (s, 1H), 7.35-7.22 (m, 3H), 5.90 (ddd, J=7.3, 10.0, 17.4 Hz, 1H), 5.38 (d, J=17.5 Hz, 1H), 5.18 (d, J=7.2 Hz, 1H), 5.15 (d, J=10.1 Hz, 1H), 0.96 (s, 9H), 0.18 (s, 3H), 0.08 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653260B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-4aa8329bf19b41b9bf83b88b5f67d166 |
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| Source note | uspto-grants-2014_02 |
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