HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646004Generated: October 29, 2026
Triphenylphosphine → Methyl 6-[2-chloro-4-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)phenyl]-1-naphthalenecarboxylate
https://huagongshe.com/reaction/646004
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | (3-(2,6-Dichlorophenyl)-5-isopropylisoxazol-4-yl)methanol | HCID 10850745 | — |
| Reactant | HCID 59264873 | HCID 59264873 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 6-[2-chloro-4-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)phenyl]-1-naphthalenecarboxylate | HCID 59264865 | — |
Reaction Steps
A mixture of methyl 6-(2-chloro-4-hydroxyphenyl)-1-naphthalenecarboxylate (0.25 g, 0.799 mmol), polymer-bound triphenylphosphine (0.27 g, 0.799 mmol), [3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methanol (0.23 g, 0.799 mmol) and 10 mL of dichloromethane was cooled to 0° C. Diisopropyl azodicarboxylate (0.16 mL, 0.799 mmol) was slowly added to the reaction mixture. The reaction mixture was stirred for 10 minutes at the above temperature and then warmed to room temperature and stirred for 18 h. The reaction mixture was filtered and the filtrate was concentrated to give oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07705028B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-667d21e6975f499eafb356a09cffd2bf |
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| Source note | uspto-grants-2010_04 |
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