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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682Generated: October 23, 2026

Triphenylphosphine → Methyl 4-(4-chromanoyloxy)-2-methoxybenzoate

https://huagongshe.com/en/reaction/1682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantChroman-4-olHCID 92890—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantMethyl 4-hydroxy-2-methoxybenzoateHCID 12532676—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(4-chromanoyloxy)-2-methoxybenzoateHCID 19691018—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of methyl 4-hydroxy-2-methoxybenzoate (364 mg, 2.0 mmol) in dry THF (1.25 mL) was added triphenylphosphine (525 mg, 2.0 mmol) and the solution was cooled to 0° C. A 500 mL volume of 4-chromanol (200 mg, 1.33 mmol) and diethyl azodicarboxylate (315 mL, 2.0 mmol) in THF was added dropwise via syringe 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-(4-chromanoyloxy)-2-methoxybenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726172
Source datasetuspto-grants-1998_03
ORD IDord-c76a22e184294ef893b6fc5df9e611d7
Source noteuspto-grants-1998_03