Ethyl bromoacetate → HCID 86597600, compound

HRID 1766692Notes

Reaction equation

HRID 1766692 reaction equation
[CH2:1]([O:8][C:9]1[CH:26]=[CH:25][C:12]([O:13][C:14]2[C:22]3[CH2:21][CH2:20][CH2:19][C:18]=3[C:17]([OH:23])=[CH:16][C:15]=2[CH3:24])=[CH:11][C:10]=1[CH:27]([CH3:29])[CH3:28])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Br[CH2:31][C:32]([O:34][CH2:35][CH3:36])=[O:33]>>[CH2:1]([O:8][C:9]1[CH:26]=[CH:25][C:12]([O:13][C:14]2[C:15]([CH3:24])=[CH:16][C:17]([O:23][CH2:31][C:32]([O:34][CH2:35][CH3:36])=[O:33])=[C:18]3[C:22]=2[CH2:21][CH2:20][CH2:19]3)=[CH:11][C:10]=1[CH:27]([CH3:29])[CH3:28])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 7748Ethyl bromoacetateHCID 23031111HCID 23031111, compound

Product 1

HCID 86597600HCID 86597600, compound

Procedure

The title compound was prepared in a similar manner to those described in Reference Example 11 using 7-(4-benzyloxy-3-isopropylphenoxy)-6-methylindan-4-ol instead of 2-hydroxy-5-(5-methyl-7-nitroindan-4-yloxy)benzaldehyde and using ethyl bromoacetate instead of benzyl bromide.

Sources & evidence

ORD record
ord-c75c50bd3926473aab84b7373135852b
Source dataset
uspto-grants-2007_06
Patent number
US07230031B2

Reaction notes

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