HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl (3S)-3-(4-hydroxyphenyl)hex-4-ynoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | (3S)-3-(4-Hydroxyphenyl)-4-hexynoic acid | HCID 59855121 | — |
| Product | Ethyl (3S)-3-(4-hydroxyphenyl)hex-4-ynoate | HCID 67087065 | — |
Reaction Steps
To a 0° C. solution of (3S)-3-(4-hydroxyphenyl)hex-4-ynoic acid (2.7 g, 13.2 mmol) in ethanol (135 mL) is added sulfuric acid (2.7 mL) and the mixture is heated at reflux for 4 hours, concentrated, diluted with water, and extracted with EtOAc (2×100 mL). The combined extracts are washed with saturated brine, dried over sodium sulfate, filtered, and concentrated to yellow oil (2.1 g, 68%). 1H NMR (400 MHz, CDCl3) δ 7.23 (d, J=8.0 Hz, 2H), 6.76 (d, J=8.0 Hz, 2H), 4.9 (bs, 1H), 4.11 (q, J=6.8 Hz, 2H), 4.04 (m, 1H), 2.60-2.75 (m, 2H), 1.82 (s, 3H), 1.21 (t, J=6.8 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383642B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-9a5edba5ad724386a06db3a0d4534a46 |
| Source note | uspto-grants-2013_02 |