Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Nitrobenzenesulfonyl chloride | HCID 7404 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | (R)-2-hydroxy-3-methoxycarbonyl-2-penten-4-olide | HCID 54688321 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22851705 | HCID 22851705 | — |
Reaction Steps
34.44 g of (R)-2-hydroxy-3-methoxycarbonyl-2-penten-4-olide are dissolved in 170 ml of toluene at 40° C., 49.4 g of p-nitrobenzenesulphonyl chloride in 160 ml of toluene are added and the whole is cooled to 5° C. Within a period of 30 minutes, 20.3 g of N-methylmorpholine are metered in at from 0 ° to 5° C. 350 ml of water are added, the toluene product phase is removed, and the aqueous phase is re-extracted twice with 100 ml of toluene. The toluene phases are washed with sodium chloride solution and with water, filtered over a small amount of silica gel and concentrated by evaporation. The residue is crystallised from ethyl acetate/cyclohexane. [α]D20 =+12.4° (3% in CHCl3), m.p. 123°-124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05625059 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-a08739a82bba4499bfe0ebe981bdd7ec |
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| Source note | uspto-grants-1997_04 |
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