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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant(3-(2,6-Dichlorophenyl)-5-isopropylisoxazol-4-yl)methanolHCID 10850745—
ReactantHCID 59264873HCID 59264873—
SolventDichloromethaneHCID 6344—
ProductMethyl 6-[2-chloro-4-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)phenyl]-1-naphthalenecarboxylateHCID 59264865—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705028B2
Source datasetuspto-grants-2010_04
ORD IDord-667d21e6975f499eafb356a09cffd2bf
Source noteuspto-grants-2010_04