HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26236Generated: October 30, 2026
Acetyl chloride → 3-Acetoxy-5-chloro-2-dodecyl-1,4-naphthoquinone
https://huagongshe.com/reaction/26236
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178442826 | HCID 178442826 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Acetoxy-5-chloro-2-dodecyl-1,4-naphthoquinone | HCID 21325243 | — |
Reaction Steps
A solution of 0.95 parts of 5-chloro-2-dodecyl-3-hydroxy-1,4-naphthoquinone in 20 parts of anhydrous tetrahydrofuran was added under nitrogen to a mixture of 0.0635 parts of dispersed sodium hydride in 40 parts of tetrahydrofuran with stirring at room temperature. After 45 minutes of stirring, a solution of 0.275 parts of acetyl chloride in 30 parts of tetrahydrofuran was added and the mixture stirred for 5 hours. The tetrahydrofuran was stripped under reduced pressure and the residue taken up in methylene chloride and then washed with water, 10% hydrochloric acid, four more times with water, dried over sodium sulfate and stripped. The resulting yellow solid was purified by column chromatography on silica gel using 1-chlorobutane as eluent. Solvent removal gave 0.9 parts of 3-acetoxy-5-chloro-2-dodecyl-1,4-naphthoquinone, m.p. 57°-59° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04148918 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-a23e3a8557d14704af10c6d5c0d72db7 |
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| Source note | uspto-grants-1979_04 |
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