HCID 10353718, compound → HCID 21436780, compound

HRID 2397883Notes

Reaction equation

HRID 2397883 reaction equation
[OH:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8]([N+:10]([O-:12])=[O:11])=[C:7]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[C:6]=2[CH:19]=1.O[C:21]1[CH:34]=CC=C(OC)[C:22]=1C(C1C=CC=CC=1)=O>>[CH:21]([O:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8]([N+:10]([O-:12])=[O:11])=[C:7]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[C:6]=2[CH:19]=1)([CH3:34])[CH3:22]

Participants

3

Reactant 2

HCID 10353718HCID 10353718, compoundHCID 21436796HCID 21436796, compound

Product 1

HCID 21436780HCID 21436780, compound

Procedure

Using the procedure described in Example 3 and starting with 5-hydroxy- 2-nitro-3 -phenylbenzofuran and isopropyl iodide one obtains 5-isopropoxy-2-nitro-3-phenylbenzofuran.

Sources & evidence

ORD record
ord-0db3c8968e3f47c59e91a446b988a593
Source dataset
uspto-grants-1977_05
Patent number
US04022908

Reaction notes

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