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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844407Generated: November 2, 2026

2,6-Dichlorophenol → HCID 86731079, compound

https://huagongshe.com/reaction/1844407

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichlorophenolHCID 6899—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 11127767HCID 11127767—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86731079HCID 86731079302.6%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946430B2
Source datasetuspto-grants-2015_02
ORD IDord-7743de142add457181450d36d711748a
Source noteuspto-grants-2015_02