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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067861Generated: November 2, 2026

Tributylphosphine → 3-(4-[2-(6,11-Dihydrodibenzo[b,e]oxepin-11-yloxy)-ethoxy]-phenyl)-2-ethoxy-propionic acid ethyl ester

https://huagongshe.com/reaction/1067861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantEthyl 2-ethoxy-3-(4-hydroxyphenyl)propanoateHCID 11791243—
ReactantHCID 21194993HCID 21194993—
SolventBenzeneHCID 241—
SolventHeptaneHCID 8900—
Product3-(4-[2-(6,11-Dihydrodibenzo[b,e]oxepin-11-yloxy)-ethoxy]-phenyl)-2-ethoxy-propionic acid ethyl esterHCID 993469537%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under a nitrogen atmosphere, 2-(6,11-dihydrodibenzo[b,e]oxepin-1-yloxy)-ethanol (256 mg, 1.0 mmol), tributylphosphine (223 mg, 1.1 mmol) and 2-ethoxy-3-(4-hydroxy-phenyl)-propionic acid ethyl ester (262 mg, 1.1 mmol) were successively dissolved in dry benzene (130 mL). Solid azodicarboxylic dipiperidine (ADDP) (278 mg, 1. 1 mmol) w as added under stirring at 0° C. to the solution. After 10 min, the reaction mixture was brought to room temperature and the stirring was continued for 16 h. Heptane (10 mL) was added to the reaction mixture and dihydro-ADDP separated out was filtered off. After evaporation of the solvent the product was purified chromatography eluting with ethyl acetate/heptane (1:4) to give 175 mg (37%) of the title compound: 1H NMR (300 MHz, CDCl3) δ1.15 (t, 3H), 1.25 (t, 3H), 2.93 (d, 2H), 3.30-3.40 (m, 1H), 3.55-3.65 (m, 1H), 3.65-3.75 (m, 1H),3.78-3.88 (m, 1H), 3.95 (t, 1H), 4. 10 (t, 2H), 4.15 (q, 2H), 4.85 (d, 1H), 5.25 (s, 1H), 6.15 (d, 1 H), 6.75 (d, 2H), 6.85-6.95 (m, 2H), 7.10 (d, 2H), 7.15-7.40 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248781B1
Source datasetuspto-grants-2001_06
ORD IDord-efd097b7b7be4d9990189dd2ee815b1b
Source noteuspto-grants-2001_06