HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464150Generated: October 30, 2026
1-Bromo-3-chloropropane → HCID 53719052, compound
https://huagongshe.com/reaction/1464150
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Ethyl cyano(3,4-dimethoxyphenyl)acetate | HCID 12814070 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53719052 | HCID 53719052 | — |
Reaction Steps
124.5 g (0.5 mol) of ethyl 3,4-dimethoxyphenylcyanoacetate in 160 ml of abs. dimethylformamide were added at 15°-20° while stirring to a suspension of 84.5 g (0.753 mol) of potassium tert-butylate in 300 ml of abs. dimethylformamide. After one hour 83.5 ml of 1-bromo-3-chloropropane were slowly added dropwise, whereby the temperature amounted to 15°-20°. After 16 hours the reaction mixture was evaporated in a high vacuum. The residue was partitioned between ether and an aqueous saturated ammonium chloride solution. The combined organic extracts were dried and evaporated under reduced pressure. The oily residue was distilled in a high vacuum, whereby 145.7 g of ethyl [γ-chloropropyl-3,4-dimethoxyphenyl]cyanoacetate were obtained, b.p. 195°-201°/80 Pa.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05302727 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-7fa6ed8faa0d43dcbf2f68cc1802b357 |
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| Source note | uspto-grants-1994_04 |
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