Acetyl chloride → HCID 54302051, compound

HRID 582213Notes

Reaction equation

Cl.[CH2:2]([C:9]1[CH2:10][C:11]2[C:16]([C:17]=1[CH2:18][CH2:19][NH2:20])=[CH:15][C:14]([O:21][CH3:22])=[CH:13][CH:12]=2)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:23](Cl)(=[O:25])[CH3:24]>>[CH2:2]([C:9]1[CH2:10][C:11]2[C:16]([C:17]=1[CH2:18][CH2:19][NH:20][C:23](=[O:25])[CH3:24])=[CH:15][C:14]([O:21][CH3:22])=[CH:13][CH:12]=2)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

Participants

Reactant 2

HCID 6367Acetyl chloride

HCID 70188030HCID 70188030, compound

Product 1

HCID 54302051HCID 54302051, compound

Procedure

Starting with 2-(2-benzyl-5-methoxy-1H-inden-3-yl) ethylamine hydrochloride and acetyl chloride, the title compound was synthesized in otherwise the same manner as Example 8 (yield 94%).

Sources & evidence

ORD record: ord-c278303cb7084cdc8a4d2519d4d0f8e0
Source dataset: uspto-grants-1999_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05922771

Reaction notes

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