Triethylamine → HCID 10546047, compound

HRID 1033495Notes

Reaction equation

HRID 1033495 reaction equation
[OH:1][CH2:2][CH2:3][N:4]1[C:12]2[C:7](=[CH:8][C:9]([Br:13])=[CH:10][CH:11]=2)[CH:6]=[CH:5]1.[Si:14](Cl)([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:16])[CH3:15].C(N(CC)CC)C>C(Cl)Cl>[Si:14]([O:1][CH2:2][CH2:3][N:4]1[C:12]2[C:7](=[CH:8][C:9]([Br:13])=[CH:10][CH:11]=2)[CH:6]=[CH:5]1)([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:16])[CH3:15]

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 28928tert-Butyldimethylsilyl chlorideHCID 106576502-(5-Bromo-1H-indol-1-yl)ethanol

Product 1

HCID 10546047HCID 10546047, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A solution of 1(2-hydroxyethyl)-5-bromoindole (6 gm, 0.025 mol), t-butyldimethylsilyl chloride (4.5 gm, 0.03 mol) and triethylamine (4.2 ml, 0.03 mol) in CH2Cl2 (60 ml) was stirred for 12 hours at room temperature. The reaction mixture was then washed twice with H2O, dried over Na2SO4, filtered and concentrated in vacuo to provide the title compound as a yellow oil. 1H NMR was consistent with the desired structure.

Workup

  1. washThe reaction mixture was then washed twice with H2O
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-944b6f8d80ec4cf78b4a44dc378cac0b
Source dataset
uspto-grants-1994_05
Patent number
US05310901

Reaction notes

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