HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260615Generated: October 26, 2026
Acetyl chloride → 1-Acetoxy-2-methylnaphthalene
https://huagongshe.com/reaction/260615
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methyl-1-naphthol | HCID 24055 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Acetoxy-2-methylnaphthalene | HCID 11805727 | 63.1% |
Reaction Steps
A solution of 9.48 g (60 mmole) of 2-methyl-1-naphthol and 8.10 g (80 mmole) of triethylamine in 50 mL of ethyl acetate was cooled to below 5° C. in an ice-bath. 5.50 g (70 mmole) of acetyl chloride was added at a rate such that the temperature did not rise about 5° C. The reaction mixture was stirred for an additional one hour, diluted with 50 mL of ethyl acetate, and washed with water then brine. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated to give an oily residue. Crystallization in hexane yielded 7.58 g (63% yield) of the title compound with a melting point of 81°-83° C. and an 1HNMR as follows: (300 MHz, DMSO-d6) δ 2.26 ) (s, 3H), 2.48 (s, 3H), 7.42 (d, 1H, J=9 Hz), 7.46-7.55 (m, 2H), 7.47-7.81 (m, 2H), 7.92 (d, 1H, J=9 Hz). The mass spectrum showed a molecular ion at m/z 200.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05529583 |
|---|
| Source dataset | uspto-grants-1996_06 |
|---|
| ORD ID | ord-78e6d1cf38c14d24b7bae736936f3e0d |
|---|
| Source note | uspto-grants-1996_06 |
|---|