2-Amino-4-phenoxybutanoic acid → HCID 21713010, compound

HRID 1111686Notes

Reaction equation

HRID 1111686 reaction equation
[NH2:1][CH:2]([CH2:6][CH2:7][O:8][C:9]1[C:18]2[C:13](=CC=CC=2)[CH:12]=[CH:11][CH:10]=1)[C:3](O)=[O:4].NC(CCOC1C=CC=CC=1)C(O)=O>>[NH2:1][CH:2]([CH2:6][CH2:7][O:8][C:9]1[CH:18]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH2:3][OH:4]

Participants

3

Reactant 2

HCID 131001282-Amino-4-phenoxybutanoic acidHCID 227550002-Amino-4-(1-naphthyloxy)butanoic acid

Product 1

HCID 21713010HCID 21713010, compound

Procedure

In the same manner but replacing 2-amino-4-(1-naphthyloxy)butanoic acid with an equivalent amount of 2-amino-4-phenoxy-butanoic acid, described by Y. Knobler, et al., J. Org. Chem., 24, 1794 (1959), 2-amino-4-phenoxy-1-butanol, γmaxCHCl3 3230-3400, is obtained. The hydrochloric acid addition salt of 2-amino-4-phenoxy-1-butanol has mp 136°-138° C., after recrystallization from methanol-diethyl ether.

Sources & evidence

ORD record
ord-05cace688f9f47f283aaf64c5f70498d
Source dataset
uspto-grants-1978_10
Patent number
US04118511

Reaction notes

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