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Methane → HCID 12968235, compound

HRID 48254
Notes
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Reaction equation

HRID 48254 reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][C:10]3[CH:32]=[C:31]([OH:33])[CH:30]=[CH:29][C:11]=3[C:12]=2[CH:13]([C:15]2[CH:20]=[CH:19][C:18]([O:21][CH2:22][CH2:23][N:24]3[CH2:28][CH2:27][CH2:26][CH2:25]3)=[CH:17][CH:16]=2)O)=[CH:4][CH:3]=1.C>>[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][C:10]3[CH:32]=[C:31]([OH:33])[CH:30]=[CH:29][C:11]=3[C:12]=2[CH2:13][C:15]2[CH:16]=[CH:17][C:18]([O:21][CH2:22][CH2:23][N:24]3[CH2:28][CH2:27][CH2:26][CH2:25]3)=[CH:19][CH:20]=2)=[CH:4][CH:3]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 297MethaneHCID 12968234[2-(4-Hydroxyphenyl)-6-hydroxybenzofuran-3-yl][4-[2-(1-pyrrolidinyl)ethoxy]phenyl]methanol

Product 1

HCID 12968235HCID 12968235, compoundYield 52.4%

Procedure

550 mg (1.2 mmol) of the product of Example 11 was reduced to the methane by the method described in Example 2. This yielded 270 mg of the title compound as an amorphous powder.

Sources & evidence

ORD record
ord-bd7aa0b2cd034660b2ef6082c537ae47
Source dataset
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06703407B1

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes