Ethyl Bromide → HCID 178467762, compound

HRID 1067725Notes

Reaction equation

HRID 1067725 reaction equation
C1(C(C2C=CC=CC=2)(C2C=CC=CC=2)[N:8]2[CH:12]=[C:11]([CH2:13][CH2:14][CH2:15][OH:16])[N:10]=[CH:9]2)C=CC=CC=1.Br[CH2:30][CH3:31]>>[NH:8]1[CH:12]=[C:11]([CH2:13][CH2:14][CH2:15][O:16][CH2:30][CH3:31])[N:10]=[CH:9]1

Participants

3

Reactant 2

HCID 6332Ethyl BromideHCID 108328403-(1-Trityl-1H-imidazol-4-YL)propan-1-OL

Product 1

HCID 178467762HCID 178467762, compound

Procedure

5 mmol of 3-(1-triphenylmethyl-1H-imidazol-4-yl)propanol and 5 mmol of bromoethane are treated as described in Example 5. The title compound is crystallized in the form of hydrogen oxalate from ethanol and diethyl ether.

Workup

  1. customThe title compound is crystallized in the form of hydrogen oxalate from ethanol and diethyl ether

Sources & evidence

ORD record
ord-fc1762935807450a9ff9c158ccc42e2c
Source dataset
uspto-grants-2001_06
Patent number
US06248765B1

Reaction notes

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