5-Bromo-1-indanone → HCID 24987022, compound

HRID 2251646Notes

Reaction equation

HRID 2251646 reaction equation
[C:1]([C:4]1[CH:5]=[C:6](B(O)O)[CH:7]=[CH:8][CH:9]=1)(=[O:3])[CH3:2].Br[C:14]1[CH:15]=[C:16]2[C:20](=[CH:21][CH:22]=1)[C:19](=[O:23])[CH2:18][CH2:17]2>>[C:1]([C:4]1[CH:5]=[C:6]([C:14]2[CH:15]=[C:16]3[C:20](=[CH:21][CH:22]=2)[C:19](=[O:23])[CH2:18][CH2:17]3)[CH:7]=[CH:8][CH:9]=1)(=[O:3])[CH3:2]

Participants

3

Reactant 2

HCID 5206955-Bromo-1-indanoneHCID 27343103-Acetylphenylboronic acid

Product 1

HCID 24987022HCID 24987022, compound

Procedure

The title compound was prepared from 3-acetylphenyl boronic acid and 5-bromo-1-indanone according to the coupling procedure as described in example 6. MS (ESI) m/z 251; HRMS: calcd for C17H14O2+H+, 251.10666; found (ESI, [M+H]+), 251.1077.

Sources & evidence

ORD record
ord-e4aaad27537645b4adaf31749c50701a
Source dataset
uspto-grants-2008_01
Patent number
US07319152B2

Reaction notes

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