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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186693Generated: November 1, 2026

Phenol → HCID 9861815, compound

https://huagongshe.com/reaction/2186693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantN,N,N',N'-TetramethylazodicarboxamideHCID 4278—
ReactantTributylphosphineHCID 13831—
ReactantHCID 22503724HCID 22503724—
SolventBenzeneHCID 241—
ProductHCID 9861815HCID 986181562.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

1,1′-Azobis(N,N-dimethylformamide) (0.34 g, 2.0 mmol) was added to a solution of 10-benzoyl-5,6,8,9,10,11,12,12a-octahydro-4H,7aH-azepino[4′,5′:4,5]pyrrolo[3,2,1-ij]quinolin-4-ol (0.45 g, 1.3 mmol), phenol (0.18 g, 1.9 mmol), and tributylphosphine (0.49 mL, 2.0 mmol) in dry benzene (4.0 mL) at room temperature under N2. The reaction mixture immediately congealed but resumed stirring upon heating to 60° C. After 5 h, the reaction was cooled to room temperature and filtered to remove white precipitate. The filtrate was concentrated under reduced pressure and purified by silica gel chromatography with heptanes/EtOAc (gradient 3:1 to 3:2) to give 0.26 g (47%) of the title compound as a beige foam. 1H NMR (CDCl3) δ 7.52-7.38, 7.32, 7.11-6.95, 5.68, 4.21-3.90, 3.69, 3.21, 2.91, 2.63, 2.34; IR (drift) 1630, 1596, 1492, 1458, 1421, 1359, 1327, 1291, 1267, 1226, 1192, 786, 750, 706, 694 cm−1; MS (ESI) 423.3 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407092B1
Source datasetuspto-grants-2002_06
ORD IDord-396a416b00bb44ddae5e3417f0f082ed
Source noteuspto-grants-2002_06