1,4-Dibromobutane → HCID 21490322, compound

HRID 1579530Notes

Reaction equation

HRID 1579530 reaction equation
Cl.[NH2:2][C:3]1[C:11]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([Cl:19])[CH:14]=2)([OH:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]=1.Br[CH2:21][CH2:22][CH2:23][CH2:24]Br>C(O)C>[Cl:19][C:15]1[CH:14]=[C:13]([C:11]2([OH:12])[C:10]3[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=3[N:4]3[CH2:21][CH2:22][CH2:23][CH2:24][N:2]=[C:3]23)[CH:18]=[CH:17][CH:16]=1

Participants

4

Reactant 2

HCID 80561,4-DibromobutaneHCID 21568707HCID 21568707, compound

Product 1

HCID 21490322HCID 21490322, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

2-Amino-3-(m-chlorophenyl)-3H-indol-3-ol hydrochloride (8.66 g) was converted to its oily base then heated under reflux with 1,4-dibromobutane (6.35 g) in ethanol (20 ml) for 4 hours. On cooling the title compound was obtained as its hydrobromide salt (2.41 g) m.p. 270°-275° C (decomp.) after recrystallization from methanol/ethyl acetate.

Workup

  1. temperaturethen heated

Sources & evidence

ORD record
ord-e72c4c7ff8f5468e93f3a47cbd7f6665
Source dataset
uspto-grants-1976_01
Patent number
US03931226

Reaction notes

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