HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38718Generated: October 25, 2026
Allyl bromide → 3-Chloro-4-(prop-2-en-1-yloxy)benzaldehyde
https://huagongshe.com/reaction/38718
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 3-Chloro-4-hydroxybenzaldehyde | HCID 17022 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Product | 3-Chloro-4-(prop-2-en-1-yloxy)benzaldehyde | HCID 4770036 | 85.6% |
Reaction Steps
To a solution of 3-chloro-4-hydroxybenzaldehyde (5.0 g, 31.9 mmol) in DMF/THF 1:3 (120 mL) is added NaH (1.67 g of a 55% dispersion in mineral oil, 38.3 mmol) in four portions. The mixture is stirred at rt for 1 h before allylbromide (9.66 g, 79.8 mmol) is added. The reaction mixture is heated to 65° C. for 18 h, diluted with water (250 mL) and extracted with diethyl ether (3×250 mL). The organic extracts are washed with water (250 mL), combined and concentrated. The remaining oil is chromatographed on silic gel with heptane/EA 4:1 to afford 4-allyloxy-3-chlorobenzaldehyde (5.37 g) as an almost colourless oil. LC: tR=0.95 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524752B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-482bcd3dcc48433ea236a8b74dc6f9fd |
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| Source note | uspto-grants-2013_09 |
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