HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175311Generated: November 2, 2026
Methanol → (E)-Methyl 3-(3-chloro-2-methylphenyl)acrylate
https://huagongshe.com/reaction/2175311
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | 3-Chloro-2-methylbenzaldehyde | HCID 13162662 | — |
| Reactant | 2-(Triphenylphosphoranylidene)acetate | HCID 21894810 | — |
| Product | (E)-Methyl 3-(3-chloro-2-methylphenyl)acrylate | HCID 86712608 | 24% |
Reaction Steps
A mixture of (2-methoxy-2-oxoethyl)triphenylphosphonium bromide (10.0 g, 24.08 mmol) in 100 mL DCM, 50 mL water and NaOH (10 N) (4.82 ml, 48.2 mmol) was vigorously shaken in a separatory funnel. The organic layer was separated and the aqueous phase was extracted with DCM. The combined organic layers were dried (MgSO4) and concentrated to give methyl 2-(triphenylphosphoranylidene)acetate (7.5 g, 93% yield) as a white solid. A solution of 3-chloro-2-methylbenzaldehyde (0.7 g, 4.53 mmol) and 2-(triphenylphosphoranylidene)acetate (1.817 g, 5.43 mmol) in MeOH (22.6 ml) was stirred at room temperature for 2 h. The mixture was concentrated and purified by flash chromatography (0-30% ethyl acetate:hexanes) to afford the title compound (0.23 g, 24% yield) as a clear colorless oil. 1H NMR (400 MHz, CDCl3) δ 7.99 (d, J=15.9 Hz, 1H), 7.47-7.40 (m, 2H), 7.17-7.15 (m, 1H), 6.33 (d, J=15.9 Hz, 1H), 3.83 (s, 3H), 2.48 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062028B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-1a3eff1ca73d4c74974c336d69c1f395 |
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| Source note | uspto-grants-2015_06 |
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