Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | HCID 14257811 | HCID 14257811 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14307643 | HCID 14307643 | — |
Reaction Steps
To a suspension of 2-(4-methoxybenzyl)-3-methyl-5-propyl-4,7-benzofurandione (from Example 28) (0.988 g, 3.05 mmol)in MeOH (23 mL) was added ethanethiol (2.5 mL). After a few minutes, the yellow quinone passed into solution giving a reddish colour. The reaction was cooled to 0° C. and solid FeCl3 (2.5 g) was added. The reaction was quenched 10% HCl and extraction with CH2Cl2 afforded the crude product which was chromatographed on silica gel (5% EtOAc/hexane) to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04778805 |
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| Source dataset | uspto-grants-1988_10 |
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| ORD ID | ord-900ca7e0ef5d4fb19dc2fba4c504678f |
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| Source note | uspto-grants-1988_10 |
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