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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393380Generated: November 1, 2026

HCID 86598325, compound → HCID 69320224, compound

https://huagongshe.com/reaction/1393380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86598325HCID 86598325—
ReactantHCID 86598326HCID 86598326—
ProductHCID 69320224HCID 69320224—

Reaction Steps

In a similar manner to Example 49-1), 3-[4-(4-hydroxyphenoxy)-phenoxy]-L-phenylalanine was synthesized by deprotecting by a conventional method from N-trifluoroacetyl-3-(4-hydroxyphenoxy)-L-phenylalanine ethyl ester via N-trifluoroacetyl-3-[4-(4-methoxyphenoxy)phenoxy]-L-phenylalanine ethyl ester. N-Trifluoroacetyl-3-[4-(4-methoxyphenoxy)phenoxy]-L-phenylalanine ethyl ester: m.p.: 67-71° C.; IR (Nujol): 3324, 1745, 1707, 1559, 1507, 1501 cm−1; APCI-MS m/z: 504 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345068B2
Source datasetuspto-grants-2008_03
ORD IDord-44db2a5aa00741b38bc00d51c3f0bfcc
Source noteuspto-grants-2008_03