HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353598Generated: October 30, 2026
4-Chloro-1-naphthol → 2-Chloro-1-(4-((4-chloronaphthyloxy)methyl)phenoxy)ethane
https://huagongshe.com/reaction/353598
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chloro-1-naphthol | HCID 11787 | — |
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | [4-(2-Chloroethoxy)phenyl]methanol | HCID 21882321 | — |
| Reactant | (4-(2-Bromoethoxy)phenyl)methanol | HCID 22482237 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-1-(4-((4-chloronaphthyloxy)methyl)phenoxy)ethane | HCID 23514395 | — |
Reaction Steps
A stirred solution of 8.4 grams (0.045 mole) of the mixture of (4-(2-bromoethoxy)phenyl)methan-1-ol and (4-(2-chloroethoxy)phenyl)methan-1-ol, 8.1 grams (0.045 mole) of 4-chloronaphthol, and 13.7 mL (0.054 mole) of tributylphosphine in 500 mL of THF was cooled in an ice bath and 12.6 grams (0.049 mole) of 1-1′-(azodicarbomyl)dipiperidine was added. Upon completion of addition, the reaction mixture was allowed to warm to ambient temperature where it stirred for 24 hours. After this time, the solvent was reduced under reduce pressure, yielding a solid. The solid was purified by column chromatography on silica gel, yielding 15 grams of crude product. The crude product was further purified by column chromatography on silca gel, yielding 6.7 grams of title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06753429B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-39008fceede749788507ff28f900e997 |
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| Source note | uspto-grants-2004_06 |
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