Water → HCID 18990361, compound

HRID 1195986Notes

Reaction equation

HRID 1195986 reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([N+:11]([O-:13])=[O:12])[C:9]=1[OH:10])[CH2:5]O.[NH:14]1[CH:18]=[CH:17][CH:16]=[CH:15]1.O>O1CCOCC1>[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([N+:11]([O-:13])=[O:12])[C:9]=1[OH:10])[CH2:5][C:15]1[NH:14][CH:18]=[CH:17][CH:16]=1

Participants

5

Conditions

Temperature
100 °C

Procedure

A solution containing 1.0 g of 3,4-dihydroxy-5-nitrobenzyl-alcohol and 5.0 ml of pyrrole in 3.0 ml of dioxane was heated for 5 h at 100° C. Water was added and the solution was extracted with dichloromethane. The solvent was evaporated and the residue was purified in a silicagel column using toluene-acetic acid-dioxane (18:1:1) mixture as an eluent. Yield 0.42 g (33%), m.p. 115°-118° C.

Workup

  1. extractionthe solution was extracted with dichloromethane
  2. customThe solvent was evaporated
  3. customthe residue was purified in a silicagel column

Sources & evidence

ORD record
ord-aa4e8a7f69114c80a220590cda8f526e
Source dataset
uspto-grants-1992_05
Patent number
US05112861

Reaction notes

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