HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 5-bromopentanoate → Benzyl 5-[(1,2-dihydro-1,2-dioxonaphth-4-yl)oxy]valerate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 5-bromopentanoate | HCID 562251 | — |
| Reactant | HCID 178516607 | HCID 178516607 | — |
| Catalyst | Silver | HCID 23954 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Benzyl 5-[(1,2-dihydro-1,2-dioxonaphth-4-yl)oxy]valerate | HCID 22647819 | — |
Reaction Steps
A mixture of benzyl 5-bromovalerate (2.27 g, 8.4 mmol) and the silver salt of 2-hydroxy-1,4-naphthoquinone (1.63 g, 5.81 mmol) in benzene (8 mL) was stirred for 48 h at 55° C. and filtered through celite. The filtrate was diluted with diethyl ether, extracted with a 20% aqueous solution of NaHSO3 then basified to pH 10-11 with Na2CO3, and extracted with CH2Cl2. Yellow solid (1.334 g, 63%). 1H NMR (CDCl3) 8.12 (d, J=7.5 Hz, 1H), 7.85 (d, J=7.7 Hz, 1H), 7.68 (t, J=7.5, 1H), 7.58 (t, J=7.7 Hz, 1H), 7.25-7.50 (m, 5H), 5.93 (s, 1H), 5.14 (s, 2H), 4.15 (t, J=5.7 Hz, 2H), 2.50 (t, J=7.0 Hz, 2H), 1.8-2.2 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06809176B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-bb94f2fc53f343eda07349bf34b93fb0 |
| Source note | uspto-grants-2004_10 |