HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166231Generated: October 26, 2026
L-Methionine → 10-(2,3-dimethoxy-5-methyl-1,4-benzoquinon-6-yl)decanoyl-L-methionine
https://huagongshe.com/reaction/2166231
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-Methionine | HCID 6137 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | p-Nitrophenyl 10-(2,3-dimethoxy-5-methyl-1,4-benzoquinon-6-yl)decanoate | HCID 12818692 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 10-(2,3-dimethoxy-5-methyl-1,4-benzoquinon-6-yl)decanoyl-L-methionine | HCID 13518527 | 62% |
Reaction Steps
To a solution of p-nitrophenyl 10-(2,3-dimethoxy-5-methyl-1,4-benzoquinon-6-yl)decanoate (237 mg, 0.5 mmol) and L-methionine (149 mg, 1 mmol) in N,N-dimethylformamide (1 ml) was added triethylamine (0.21 ml, 1.5 mmol). The mixture was stirred at room temperature for 16 hours. After removal of the solvent, the residue was dissolved in ethyl acetate (10 ml) and the solution was washed with 1N hydrochloric acid (5 ml×3) and saturated aqueous sodium chloride (5 ml×3) in that order and dried over anhydrous sodium sulfate. The solvent was then distilled off under reduced pressure and the residue was chromatographed on a column of silica gel (7 g). Elution was carried out with chloroform-methanol (4:1, v/v) and with chloroform-methanol-acetic acid (32:8:1, v/v) in the order mentioned. The fractions containing the desired compound were combined and the solvent was distilled off under reduced pressure to give 10-(2,3-dimethoxy-5-methyl-1,4-benzoquinon-6-yl)decanoyl-L-methionine (150 mg), melting at 83°-85° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04943645 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-0cd430a74cc04b6d87caaf5bc70d862e |
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| Source note | uspto-grants-1990_07 |
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