HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331247Generated: October 30, 2026
Triethyl phosphonoacetate → Ethyl (5-fluoro-3,4-dihydronaphthalen-1-yl)acetate
https://huagongshe.com/reaction/331247
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethyl phosphonoacetate | HCID 13345 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Fluoro-1,2,3,4-tetrahydronaphthalen-1-one | HCID 15491038 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl (5-fluoro-3,4-dihydronaphthalen-1-yl)acetate | HCID 86641634 | — |
Reaction Steps
To a suspension of 60% sodium hydride (5.00 g) in toluene (250 ml) was added dropwise ethyl diethylphosphonoacetate (23.9 ml) under ice-cooling, and the mixture was stirred at room temperature for 1 hr. Then, a solution of 5-fluoro-3,4-dihydro-2H-naphthalen-1-one (18.0 g) in toluene (50 ml) was added dropwise, and the mixture was stirred at 80° C. for 3 hr. After cooling to room temperature, the reaction mixture was poured into ice water, and the mixture was extracted with toluene. The extract was washed with water and saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give ethyl (5-fluoro-3,4-dihydronaphthalen-1-yl)acetate (17.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08877779B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-134402ae0f6c4ee2b6a3e08df6335f40 |
|---|
| Source note | uspto-grants-2014_11 |
|---|