HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742382Generated: October 31, 2026
3-Chloropropionyl chloride → 6-(3-Chloropropionyl)-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene
https://huagongshe.com/reaction/1742382
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloropropionyl chloride | HCID 69364 | — |
| Reactant | 1,1,4,4-Tetramethyltetralin | HCID 81186 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-(3-Chloropropionyl)-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene | HCID 14726511 | — |
Reaction Steps
73.5 g (0.55 mole) of anhydrous aluminum chloride were added a little at a time, at 0°-5° C., to a solution of 70 g (0.55 mole) of 3-chloropropionyl chloride in 200 ml of methylene chloride, after which a solution of 94 g (0.5 mole) of 1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene in 200 ml of methylene chloride was added dropwise at the same temperature. The mixture was stirred overnight at room temperature, poured onto 1 l of ice/water and extracted with 3 times 300 ml of methylene chloride. The combined organic phases were washed with saturated sodium bicarbonate solution and water, dried over magnesium sulfate and evaporated down. 138 g of 6-(3-chloropropionyl)-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene remained as an oil. The structure was determined by H-NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05338749 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-363bd4f2da0c4f37af87ae2999fa07a5 |
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| Source note | uspto-grants-1994_08 |
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