HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521475Generated: October 26, 2026
Triphenylphosphine → HCID 44482419, compound
https://huagongshe.com/reaction/521475
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Hydroxy-4-methylbenzoic acid | HCID 68512 | — |
| Reactant | m-Chlorophenethylic alcohol | HCID 78856 | — |
| Reactant | 2-Aminoindane-2-carboxylic acid | HCID 250936 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 44482419 | HCID 44482419 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328071B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-1f36c27a8013498bb0835c384846f1fa |
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| Source note | uspto-grants-2016_05 |
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