HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium hydroxide, monohydrate → (+)-(1R)-1-[5-(3-chlorophenyl)-[1,2,4]oxadiazol-3-yl]ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | (+)-(1R)-1-[5-(3-chlorophenyl)-[1,2,4]oxadiazol-3-yl]ethyl acetate | HCID 57837970 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | (+)-(1R)-1-[5-(3-chlorophenyl)-[1,2,4]oxadiazol-3-yl]ethanol | HCID 57837962 | 97% |
Reaction Steps
7.13 g (26.7 mmol) (+)-(1R)-1-[5-(3-chlorophenyl)-[1,2,4]oxadiazol-3-yl]ethyl acetate and 2.33 g (56.7 mmol) lithium hydroxide monohydrate were mixed with 1:1 THF/Water (100 mL) and stirred for 18 h. Reducing the volume of the mixture in vacuo to about ½, followed by dilution with brine and extraction with ethyl acetate. 5.8 g (97%) of the title compound was obtained after evaporation and drying. 1H NMR: 8.14 (s, 1 H), 8.02 (d, 1 H), 7.57 (d, 1 H), 7.47 (t, 1 H), 5.04-5.14 (m, 1 H), 2.42 (br s, 1 H), 1.67 (d, 3 H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07585881B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-508d2038566446659252a801c9103d97 |
| Source note | uspto-grants-2009_09 |