HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787130Generated: October 29, 2026
HCID 23114101, compound → HCID 52935173, compound
https://huagongshe.com/reaction/1787130
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 23114101 | HCID 23114101 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 52935173 | HCID 52935173 | 34% |
Reaction Steps
A suspension of 3-(4-isopropylphenyl)-4,6-dimethyl-2,3-dihydro-1-benzofuran-5-amine obtained in Reference Example 32 (22.5 g, 80 mmol) and (2S, 3S)-(4′-methyl)-tartranilic acid (19.14 g, 80 mmol) in ethanol (480 mL) was heated at 85° C. for dissolution. The solution was cooled to 0° C. for 2 hours, and the precipitated crystals were taken. The crystals were washed with cold ethanol, and then were dried under reduced pressure. The obtained crystals were suspended in a 2 N aqueous sodium hydroxide solution (400 mL), which was extracted with diethyl ether. The extract was washed with a saturated sodium hydrogen carbonate solution and a saturated brine, and then was dried over sodium sulfate. The solvent was distilled off under reduced pressure to obtain 9.44 g (yield 34%) of the title compound as an oily matter. The obtained oily matter was, if necessary, crystallized with cold hexane. Melting point: 53-55° C. [α]D20=+64.0° (c=0.44, chloroform).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07507841B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-20f2e46b71124d74bb5bae7fedc8f625 |
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| Source note | uspto-grants-2009_03 |
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