HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Benzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)acetic acid | HCID 18177932 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthylacetate | HCID 18792286 | — |
Reaction Steps
730 mg (0.024 mol) of sodium hydride (80 and 100 ml of DMF were introduced into a three-necked flank under a nitrogen stream. A solution of 5 g (0.02 mol) of 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthylacetic acid in 40 ml of DMF was added dropwise and the mixture was stirred until the gaseous emission ceased. 2.9 ml (0.024 mol) of benzyl bromide were then added and the mixture was stirred at room temperature for 4 hours. The reaction medium was poured into water, and extracted with ethyl acetate. The organic phase was decanted off, dried over magnesium sulfate and evaporated. 6.7 g (100%) of the expected ester were recovered in the form of a slightly yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05709867 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-ef9d103de7344601a737fc0d84aab076 |
| Source note | uspto-grants-1998_01 |