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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181826Generated: November 1, 2026

Dichloromethane → 5-[(4-Hydroxyphenyl)sulfonyl]-6-methyl-5,6-dihydrophenanthridin-9-ol

https://huagongshe.com/reaction/2181826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBoron TrichlorideHCID 25135—
Reactant9-Methoxy-5-[(4-methoxyphenyl)sulfonyl]-6-methyl-5,6-dihydrophenanthridineHCID 22482320—
CatalystTetrabutylammonium IodideHCID 67553—
Product5-[(4-Hydroxyphenyl)sulfonyl]-6-methyl-5,6-dihydrophenanthridin-9-olHCID 1172646356%

Reaction Steps

The title compound was prepared from 9-methoxy-5-[(4-methoxyphenyl)sulfonyl]-6-methyl-5,6-dihydrophenanthridine (0.35 g, 0.89 mmol), tetrabutylammonium iodide (0.82 g, 2.2 mmol), and 1 M boron trichloride in dichloromethane (4.44 mL, 4.44 mmol) according to the procedure and in the same manner as described in Example 35, Step b. The crude product was purified by flash column chromatography on silica gel, eluting with a mixture of ethyl acetate-hexane (3:7 to 1:1 gradient), to yield 5-[(4-hydroxyphenyl)sulfonyl]-6-methyl-5,6-dihydrophenanthridin-9-ol as a solid (0.18 g, 56%), m.p. 212° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894061B2
Source datasetuspto-grants-2005_05
ORD IDord-1b6f3752e19b4774a9c46b9473293ec5
Source noteuspto-grants-2005_05