Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718442Generated: October 29, 2026

Triphenylphosphine → HCID 118307721, compound

https://huagongshe.com/reaction/718442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
Reactant4-Methylphenethyl alcoholHCID 95294—
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 118307721HCID 11830772130.6%

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-(p-tolyl)ethanol (29.1 mg, 0.213 mmol) and Ph3P-resin (55.8 mg, 0.213 mmol) in THF (2 mL) was added DEAD (0.014 mL, 0.085 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-(4-methylphenethoxy)phenyl)pyridin-3-yl)acetic acid (7.3 mg, 0.013 mmol, 30.6% yield). 1H NMR (500 MHz, DMSO-d6) δ 7.17 (d, J=7.7 Hz, 3H), 7.09 (d, J=8.1 Hz, 2H), 7.02-6.93 (m, 3H), 5.80 (br. s., 1H), 4.25-4.13 (m, 2H), 2.96 (t, J=6.2 Hz, 2H), 2.41 (s, 3H), 2.24 (s, 3H), 2.03 (s, 3H), 1.21 (br. s., 2H), 1.09 (s, 9H), 0.77 (s., 3H), 0.62 (s., 3H). 6H of piperidine were not resolved. LCMS (M+H)=559.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193720B2
Source datasetuspto-grants-2015_11
ORD IDord-96ef994ae2224bbcb428bae45c3b6ce3
Source noteuspto-grants-2015_11