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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677Generated: October 26, 2026

Triphenylphosphine → Methyl 4-(cis-2-phenyl-1-cyclohexanoyloxy)-2-methoxybenzoate

https://huagongshe.com/reaction/1677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantrel-(1R,2S)-2-PhenylcyclohexanolHCID 102793—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantMethyl 4-hydroxy-2-methoxybenzoateHCID 12532676—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(cis-2-phenyl-1-cyclohexanoyloxy)-2-methoxybenzoateHCID 22883080—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of methyl 4-hydroxy-2-methoxybenzoate (310 mg, 1.7 mmol) in dry THF (1.25 mL) was added triphenylphosphine (446 mg, 1.7 mmol) and the solution was cooled to 0° C. A 500 mL volume of trans-2-phenyl-1-cyclohexanol (200 mg, 1.35 mmol) and diethyl azodicarboxylate (319 μL, 2.02 mmol) in THF was added dropwise via addition funnel over 0.5 h. The reaction was filtered and the solvent was removed under reduced pressure. The residue was chromatographed on a silica gel column packed in 92:8 hexanes:EtOAc and eluted with same. The appropriate fractions were combined and the solvent removed under reduced pressure to afford methyl 4-(cis-2-phenyl-1-cyclohexanoyloxy)-2-methoxybenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726172
Source datasetuspto-grants-1998_03
ORD IDord-e05a7f6ef00b40218847ea8339f5616a
Source noteuspto-grants-1998_03