Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 12001833 | HCID 12001833 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57587036 | HCID 57587036 | — |
Reaction Steps
A solution containing 39.8 mg (0.08 mmol) of (S)-(+)-N-acetyl-2,4,6-tribromo-5-methoxytryptophan methyl ester (4) dissolved in 2.5 mL of N,N-dimethylformamide was charged with 36.5 mg (0.26 mmol) of potassium carbonate and subsequently with 0.13 mL (d=1.398, 1.51 mmol) of allyl bromide. The mixture was stirred at room temperature for 30 minutes. The reaction solution was charged with water and subjected to extraction with ethyl acetate. The organic phase was washed with a saturated saline and dried over anhydrous sodium sulfate. Then, the solvent was distilled off under reduced pressure to obtain yellow oil. Purification by column chromatography using silica gel as a carrier and chloroform as an elution solvent was performed to obtain the substance of interest (6) at a yield of 42.4 mg (99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07659304B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-9e0e073931554504b0a17f44d8966ca7 |
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| Source note | uspto-grants-2010_02 |
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