Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521475Generated: October 26, 2026

Triphenylphosphine → HCID 44482419, compound

https://huagongshe.com/reaction/521475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-Hydroxy-4-methylbenzoic acidHCID 68512—
Reactantm-Chlorophenethylic alcoholHCID 78856—
Reactant2-Aminoindane-2-carboxylic acidHCID 250936—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
SolventTetrahydrofuranHCID 8028—
ProductHCID 44482419HCID 44482419—

Reaction Conditions

Temperature0 °C

Reaction Steps

The synthesis was carried out on 0.15 g of PL Wang resin (1.7 mmol/g). The attachment of 2-amino-indane-2-carboxylic acid and the acylation with 3-hydroxy-4-methylbenzoic acid were performed as in described in example 173. After the acylation step, the resin was washed with THF and a solution of triphenylphosphine (10 equivalents) and 2-(3-chlorophenyl)-ethanol (10 equivalents) in THF was added to the resin. The slurry was cooled to 0° C., DIAD (10 equivalents) was added to the cooled mixture, and the reaction mixture was shaken overnight at room temperature. The resin was washed with DCM. The compound was cleaved, isolated and purified as in described in example 173. Yield: 2.3 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328071B2
Source datasetuspto-grants-2016_05
ORD IDord-1f36c27a8013498bb0835c384846f1fa
Source noteuspto-grants-2016_05