4-tert-Butylbenzyl alcohol → HCID 22253133, compound

HRID 1351439

Reaction equation

HRID 1351439 reaction equation
[C:1]([C:5]1[CH:12]=[CH:11][C:8]([CH2:9][OH:10])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[ClH:13].[NH2:14][CH2:15][C:16](=[O:22])[CH2:17][CH2:18][C:19](O)=[O:20]>>[ClH:13].[NH2:14][CH2:15][C:16](=[O:22])[CH2:17][CH2:18][C:19]([O:10][CH2:9][C:8]1[CH:7]=[CH:6][C:5]([C:1]([CH3:4])([CH3:2])[CH3:3])=[CH:12][CH:11]=1)=[O:20]

Participants

3

Reactant 2

HCID 134164-tert-Butylbenzyl alcoholHCID 123608Aminolevulinic Acid Hydrochloride

Product 1

HCID 22253133HCID 22253133, compound

Procedure

From 4-t-butylbenzyl alcohol (5.0 g; 30 mmol) and 5-amino-4-oxopentanoic acid hydrochloride (1.0 g; 6.0 mmol). The reaction was complete after 2 days. The yield was 0.84 g (52%).

Sources & evidence

ORD record
ord-e8e786ab56954dd790fd855528c28533
Source dataset
uspto-grants-2007_05
Patent number
US07217736B2

Linked notes

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