HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 1-Amino-2-naphthalenethiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-Amino-2-naphthol | HCID 14535 | — |
| Reactant | Sodium Lauryl Sulfate | HCID 3423265 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Amino-2-naphthalenethiol | HCID 113314 | 73% |
Reaction Steps
5 mmol of 1-aminonaphthalene-2-ol was added to 20 mL of water, and 20 mg of sodium dodecylsulfate was added while agitating to obtain a uniform mixture. 7.5 mmol of acetic anhydride was added for 5 minutes. An acetylated product was precipitated in in 5-10 minutes. The precipitation product was filtrated and rinsed with 1 ml of water twice followed by drying under vacuum. A non-precipitated reaction mixture was extracted with 25 ml of ethyl acetate twice. The separated organic layer was dried with anhydrous sodium sulfate, and a solvent was removed using a rotatary evaporator under a reduced pressure to obtain 1-aminonaphthalene-2-thiol at a yield of 73%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07968715B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-67cb42ab285f47feaa19e3083698696a |
| Source note | uspto-grants-2011_06 |