Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Chloro-3-methoxy-1,4-naphthalenedione | HCID 27459 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Product | 2-Chloro-3-dodecyl-1,4-naphthoquinone | HCID 103050 | 4.6% |
| Product | HCID 20403098 | HCID 20403098 | 12.3% |
Reaction Steps
To 0.20 g (1.50 mmoles) of AlCl3 in 20 mL of THF was added 6.80 g (4.74 mmoles, 0.697 mmoles/g) of dodecyl MgBr. This mixture was added dropwise to 0.789 g (4.49 mmoles) of 2-methoxy-3-chloro-1,4-naphthoquinone and 0.529 g (3.89 mmoles) of ZnCl2 in 50 mL of THF. The mixture was stirred overnight. The green solution was poured into 100 mL of NH4Cl solution, extracted with 3×50 mL of ether, dried over MgSO4, filtered, and solvent was removed. The residue was flash-chromatographed (90% toluene/hexane as eluant) to give 0.075 g (0.021 mmoles, 4.6%) of 2-dodecyl-3-chloronaphthoquinone and 0.246 g (0.55 mmoles, 12.3%) of 2-dodecyl-3-methoxynaphthoquinone. 1H NMR (δ, CDCl3): 8.05 (m,2H), 7.65 (m,2H), 4.10 (s,3H), 2.55 (m,2H), 1.3 (br. s,20H), 0.85 (m,3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04507241 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-0685d50eeab4447ca8edd889c3931111 |
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| Source note | uspto-grants-1985_03 |
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