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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718446Generated: October 29, 2026

2-Phenylethanol → HCID 118307751, compound

https://huagongshe.com/reaction/718446

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PhenylethanolHCID 6054—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant(S)-ethyl 2-(tert-butoxy)-2-(4-(4,4-dimethylpiperidin-1-yl)-5-(4-hydroxyphenyl)-2,6-dimethylpyridin-3-yl)acetateHCID 118314205—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118307751HCID 11830775119.79%

Reaction Steps

To a stirred solution of (S)-ethyl 2-(tert-butoxy)-2-(4-(4,4-dimethylpiperidin-1-yl)-5-(4-hydroxyphenyl)-2,6-dimethylpyridin-3-yl)acetate (20 mg, 0.043 mmol), 2-phenylethanol (26.1 mg, 0.213 mmol) and Ph3P-resin (55.8 mg, 0.213 mmol) in THF (2 mL) was added DEAD (0.020 mL, 0.128 mmol) at rt. After 18 h, mixture was filtered to remove polymer, concentrated and treated with 1N NaOH (0.854 mL, 0.854 mmol) in MeOH (1 mL) at 75° C. for 16 h. Mixture was then cooled and purified by prep-HPLC to afford (S)-2-(tert-butoxy)-2-(4-(4,4-dimethylpiperidin-1-yl)-2,6-dimethyl-5-(4-phenethoxyphenyl)pyridin-3-yl)acetic acid (4.6 mg, 8.44 μmol, 19.79% yield). 1H NMR (500 MHz, DMSO-d6) δ 7.38-7.29 (m, 4H), 7.27-7.17 (m, 2H), 7.08-6.93 (m, 3H), 5.70 (br. s., 1H), 4.32-4.18 (m, 2H), 3.51-3.42 (m, 2H), 3.06 (d, J=7.0 Hz, 1H), 2.81-2.68 (m, 1H), 2.43 (s, 3H), 2.17 (d, J=13.2 Hz, 1H), 2.05 (s, 3H), 1.96-1.90 (m, 1H), 1.50 (br. s., 1H), 1.29 (br. s., 1H), 1.15 (d, J=11.7 Hz, 1H), 1.11 (s, 9H), 1.01 (d, J=11.0 Hz, 1H), 0.85 (br. s., 3H), 0.62 (br. s., 3H). LCMS (M+H)=545.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193720B2
Source datasetuspto-grants-2015_11
ORD IDord-ef47c743e2cd4fc4aafcd12354a62854
Source noteuspto-grants-2015_11