Phenylacetyl chloride → HCID 53893497, compound

HRID 224335

Reaction equation

[C:1]1([CH2:7][C:8](Cl)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.NCC[C:14]1[CH:15]=[C:16]2[C:20](=[CH:21][C:22]=1[CH3:23])[CH2:19][CH2:18][CH2:17]2>>[C:1]1([CH2:7][C:8]([C:14]2[CH:15]=[C:16]3[C:20](=[CH:21][C:22]=2[CH3:23])[CH2:19][CH2:18][CH2:17]3)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

Reactant 2

HCID 7679Phenylacetyl chloride

HCID 124261245-Aminoethyl-6-methylindan

Product 1

HCID 53893497HCID 53893497, compound

Procedure

Phenylacetyl chloride was reacted with 5-aminoethyl-6-methylindan to produce the desired product. After recrystallization from benzene it melted at 125.5°-127° C.

Sources & evidence

ORD record: ord-646632205a394532b139660e38b68696
Source dataset: uspto-grants-1980_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04232014

Linked notes

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