HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365489Generated: October 30, 2026
Water → ethyl 2-(3,4-dihydronaphthalen-2-yl)acetate
https://huagongshe.com/reaction/365489
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Tetralone | HCID 68266 | — |
| Product | ethyl 2-(3,4-dihydronaphthalen-2-yl)acetate | HCID 313346 | — |
Reaction Steps
A solution of 56 g (0.25 mol) of triethyl phosphonoacetate in 70 ml of tetrahydrofuran (THF) is added dropwise to a suspension, maintained at 0° C., of 6 g (0.25 mol) of NaH in 600 ml of anhydrous THF under a nitrogen atmosphere. The mixture is then stirred at 10° C. for 30 minutes, cooled to 0° C., and then treated, dropwise, with a solution of 36.52 g (0.25 mol) of β-tetralone in 50 ml of anhydrous THF. After stirring for 3 hours at 20° C., the mixture is hydrolysed, at 0° C., with 200 ml of water. The solvent is evaporated off under reduced pressure and the residue is extracted with dichloromethane (CH2Cl2)(3×200 ml). The combined organic phases are washed with saturated NaCl solution, dried and concentrated to yield an oily brown residue. Distillation under a partial vacuum allows the title compound to be obtained in the form of a colourless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06127396 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-3c7194b7bbca4caf8c0d3431ee2c7bd3 |
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| Source note | uspto-grants-2000_10 |
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