HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357010Generated: October 30, 2026
4-Methylmorpholine → 1H-Inden-2-amine, 5-bromo-2,3-dihydro-, (2R)-
https://huagongshe.com/reaction/2357010
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 5-Bromo-2,3-dihydro-1H-inden-2-amine--hydrogen bromide (1/1) | HCID 12192057 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1H-Inden-2-amine, 5-bromo-2,3-dihydro-, (2R)- | HCID 11275870 | 73.5% |
Reaction Steps
25 g of 5-bromo-indan-2-ylamine hydrobromide (85.32 mmol) and 9.85 ml of 4-methylmorpholin (89.59 mmol) were dissolved in 53 ml of methanol. The mixture was heated to 60° C. and a solution of 25.77 g of (1S)-(+)-campher-10-sulfonic acid (110.92 mmol) in 42 ml of methanol added within 25 minutes. The reaction mixture was stirred for 10 minutes at 60° C. and then allowed to cool down to room temperature over a 2 h time period, with stirring continuing for another 2 h. The precipitate was filtered, washed twice with 20 ml of ethyl acetate/methanol (2:1) and 20 ml of water, and finally dried at 50° C. under vacuo for 15 h to give 13.3 g of the salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759397B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-f84b02992312456cbf46c72a72929f63 |
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| Source note | uspto-grants-2010_07 |
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