HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844407Generated: November 1, 2026
2,6-Dichlorophenol → HCID 86731079, compound
https://huagongshe.com/reaction/1844407
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dichlorophenol | HCID 6899 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 11127767 | HCID 11127767 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86731079 | HCID 86731079 | 302.6% |
Reaction Steps
To a solution of 2,6-dichlorophenol (14.9 mg, 0.091 mmol) in THF (1.5 mL) was added (R)-2-(4-hydroxybutan-2-yl)isoindoline-1,3-dione (20 mg, 0.091 mmol) and triphenylphosphine (47.9 mg, 0.182 mmol) and the reaction mixture was cooled to 0° C. in an ice/water bath. DIAD (0.035 mL, 0.182 mmol) was added drop wise and the reaction mixture was stirred at 0° C. for 1 h. The reaction mixture was allowed to warm to rt and was stirred at rt overnight. The reaction mixture was concentrated under vacuum to yield a yellow oil that was diluted with a minimal amount of DCM, loaded onto a 12 g ISCO column and purified by ISCO. Intermediate 13A (0.1003 g, 96% yield) was isolated as a clear oil. LC-MS (ESI) 365 (M+H), RT=2.84 min (Method A). NMR indicated that the final product contained reduced DIAD.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946430B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-7743de142add457181450d36d711748a |
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| Source note | uspto-grants-2015_02 |
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