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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389172Generated: October 30, 2026

2-Amino-2-(6-(4-phenoxyphenoxy)naphthalen-2-yl)propane-1,3-diol → 2-Amino-2-(6-(4-(pentyloxy)phenoxy)naphthalen-2-yl)propane-1,3-diol

https://huagongshe.com/reaction/2389172

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-2-(6-(4-phenoxyphenoxy)naphthalen-2-yl)propane-1,3-diolHCID 67423693—
Reactant2,2-Dimethyl-5-(6-(4-(pentyloxy)phenoxy)naphthalen-2-yl)-1,3-dioxan-5-amineHCID 67425477—
Product2-Amino-2-(6-(4-(pentyloxy)phenoxy)naphthalen-2-yl)propane-1,3-diolHCID 6741314955%

Reaction Steps

2-amino-2-(6-(4-(pentyloxy)phenoxy)naphthalen-2-yl)propane-1,3-diol was synthesized as per 2-amino-2-(6-(4-phenoxyphenoxy)naphthalen-2-yl)propane-1,3-diol (Example 245) in 55% yield using 2,2-dimethyl-5-(6-(4-(pentyloxy)phenoxy)naphthalen-2-yl)-1,3-dioxan-5-amine as starting material. MS: m/z=418.45 [M+Na+]. 1H NMR (MeOD) δ: 7.88-7.94 (m, 2H), 7.78 (d, J=8.8 Hz, 1H), 7.51 (dd, J=8.8, 2.0 Hz, 1H), 7.30 (dd, J=9.0, 2.5 Hz, 1H), 7.17 (d, J=2.3 Hz, 1H), 7.01-7.07 (m, 2H), 6.94-7.01 (m, 2H), 4.05-4.12 (m, 2H), 3.96-4.02 (m, 4H), 1.70-1.85 (m, 2H), 1.37-1.54 (m, 4H), 0.92-1.01 (m, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269043B2
Source datasetuspto-grants-2012_09
ORD IDord-5cdf8f8546644f4a9c478bf94a6b59d9
Source noteuspto-grants-2012_09