4-Nitrobenzyl alcohol → 4-Nitrobenzyl 5-amino-4-oxopentanoate Hydrochloride

HRID 1182002

Reaction equation

HRID 1182002 reaction equation
[N+:1]([C:4]1[CH:11]=[CH:10][C:7]([CH2:8][OH:9])=[CH:6][CH:5]=1)([O-:3])=[O:2].[ClH:12].[NH2:13][CH2:14][C:15](=[O:21])[CH2:16][CH2:17][C:18](O)=[O:19]>>[ClH:12].[NH2:13][CH2:14][C:15](=[O:21])[CH2:16][CH2:17][C:18]([O:9][CH2:8][C:7]1[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:11][CH:10]=1)=[O:19]

Participants

3

Reactant 2

HCID 692754-Nitrobenzyl alcoholHCID 123608Aminolevulinic Acid Hydrochloride

Product 1

HCID 222531494-Nitrobenzyl 5-amino-4-oxopentanoate Hydrochloride

Procedure

From 4-nitrobenzyl alcohol (5.0 g; 33 mmol) and 5-amino-4-oxopentanoic acid hydrochloride (1.0 g; 6.0 mmol). The reaction was complete after 15 min at 135° C. The yield was 0.95 g (52%).

Sources & evidence

ORD record
ord-2d997a97e15742e6a38bcd2a0f0bbec7
Source dataset
uspto-grants-2007_10
Patent number
US07287646B2

Linked notes

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