HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222202Generated: October 29, 2026
Hydrazine → rac-(1R,2R)-2-methoxy-2,3-dihydro-1H-inden-1-amine
https://huagongshe.com/reaction/222202
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 2-[(1R,2R)-2-methoxy-2,3-dihydro-1H-inden-1-yl]-1H-isoindole-1,3(2H)-dione | HCID 66617989 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | rac-(1R,2R)-2-methoxy-2,3-dihydro-1H-inden-1-amine | HCID 28109794 | 66.9% |
Reaction Steps
To a mixture of 2-[(1R,2R)-2-methoxy-2,3-dihydro-1H-inden-1-yl]-1H-isoindole-1,3(2H)-dione (4.13 g, 0.00141 mol) in ethanol (3.38 mL) under an atmosphere of argon was added hydrazine (0.0442 mL, 0.0580 mol). The reaction mixture was allowed to stir at rt overnight. White solid byproduct crashed out of solution. TLC showed no starting material. The reaction mixture was concentrated, and the residue was suspended in DCM and filtered. The filtrate was concentrated in vacuo. 1H NMR showed that the reaction had not gone to completion. The yellow oil was therefore stirred at reflux for 3 h. LCMS confirmed reaction was complete. The reaction mixture was cooled to rt, concentrated in vacuo, triturated with DCM, filtered, and the filtrate was concentrated in vacuo to give product as a yellow oil (0.154 g, 64%). LC/MS: Rt=0.68 min, ES+ 164 (AA standard).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207177B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-f67904c9bf2a49bb8209904c582c38e1 |
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| Source note | uspto-grants-2012_06 |
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