HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297980Generated: October 30, 2026
Potassium Carbonate → HCID 54445672, compound
https://huagongshe.com/reaction/2297980
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | 1,3-Benzodioxole, 5-(chloromethyl)- | HCID 88713 | — |
| Reactant | HCID 18337555 | HCID 18337555 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54445672 | HCID 54445672 | — |
Reaction Steps
To a solution of 2(R)-(4-methoxy-2,3,6-trimethylbenzenesulfonylamino)-3-hydroxypropionic acid (27.9 g, 87.9 mmol) in dimethylformamide (280 mL) at 0° C., was added potassium carbonate (72.9 g, 527 mmol) and a solution of 3,4-methylenedioxybenzyl chloride ((60 g, 170.8 mmol, 50% (w/w)) in methylene chloride. After 2 h, lithium iodide (5.88 g, 44 mmol) was added and the reaction mixture was warmed to rt. over 2 h. After 6 h, the reaction mixture was partitioned between ethyl acetate (600 mL) and water (250 mL). The organic layer was separated, dried over magnesium sulfate and concentrated in vacuo. The crude residue was chromatographed (300 g SiO2, 15% ethyl acetate-hexanes) to afford 2(R)-(4-methoxy-2,3,6-trimethylbenzenesulfonylamino)-3-hydroxypropionic acid 3,4-methylenedioxybenzyl ester (38.4 g) which was taken directly into the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06492394B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-2edd2ba24b07456084b37a530d64a731 |
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| Source note | uspto-grants-2002_12 |
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