1-(2-(Tert-butoxycarbonylamino)-5-methoxyphenyl]-2-butanone → 2-ethyl-5-methoxy-1H-indole

HRID 2303519Notes

Reaction equation

HRID 2303519 reaction equation
C(OC([NH:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][C:10]=1[CH2:17][C:18](=O)[CH2:19][CH3:20])=O)(C)(C)C>C(Cl)Cl.FC(F)(F)C(O)=O>[CH2:19]([C:18]1[NH:8][C:9]2[C:10]([CH:17]=1)=[CH:11][C:12]([O:15][CH3:16])=[CH:13][CH:14]=2)[CH3:20]

Participants

4

Reactant 1

HCID 105178251-(2-(Tert-butoxycarbonylamino)-5-methoxyphenyl]-2-butanone

Product 1

HCID 107024052-ethyl-5-methoxy-1H-indoleYield 58%

Reagents, catalysts & solvents 2

HCID 6344DichloromethaneSolventHCID 6422Trifluoroacetic acidSolvent

Procedure

1-[2-(tert-Butoxycarbonylamino)-5-methoxyphenyl]-2-butanone (7.33 g, 0.025 mol) in 120 mL of CH2Cl2 and 20 mL of trifluoroacetic acid was stirred for 20 hours, washed with water, NaHCO3 solution and the product chromatographed on silica (eluted with 20% EtOAc/hexane) to give 2.54 g (58% yield) of 2-ethyl-5-methoxy-1H-indole as a white solid, mp 49-50° C.

Workup

  1. washwashed with water, NaHCO3 solution
  2. customthe product chromatographed on silica (eluted with 20% EtOAc/hexane)

Sources & evidence

ORD record
ord-46629abe0b214a0282303af10efa6791
Source dataset
uspto-grants-2002_08
Patent number
US06433001B1

Reaction notes

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