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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361529Generated: October 30, 2026

Triphenylphosphine → Methyl 3-{(1S)-2-methoxy-(1-methylethyl)oxy}-5-{[(2-methylphenyl)methyl]oxy}benzoate

https://huagongshe.com/reaction/1361529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant(R)-(-)-1-Methoxy-2-propanolHCID 2733589—
ReactantMethyl 3-hydroxy-5-{[(2-methylphenyl)methyl]oxy}benzoateHCID 21074227—
SolventMethyl ChlorideHCID 6327—
ProductMethyl 3-{(1S)-2-methoxy-(1-methylethyl)oxy}-5-{[(2-methylphenyl)methyl]oxy}benzoateHCID 5912715655%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

A stirred suspension of methyl 3-hydroxy-5-{[(2-methylphenyl)methyl]oxy}benzoate (15.3 g, 56.25 mmol) and triphenyl phosphine (14.4 g, 55 mmol) in dry chloromethane (900 ml) was cooled in an ice-bath and diisopropyl azodicarboxylate (11.88 ml, 55 mmol) was added dropwise. The reaction mixture was stirred at 0-5° C. for 30 minutes and (R)-methoxy-propan-2-ol was added dropwise. The reaction mixture was stirred at ambient temperature for 16 hours, and filtered through diatomaceous earth. The filtrate was evaporated and purified by column chromatograph on silica gel eluting with 10% ethyl acetate in iso-hexane to give the desired compound (10.7 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880012B2
Source datasetuspto-grants-2011_02
ORD IDord-eade8ab01b4e493d90e86fc781a77c34
Source noteuspto-grants-2011_02