HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426027Generated: November 2, 2026
1,2,3,4-Tetrahydro-1-naphthylamine → HCID 11551484, compound
https://huagongshe.com/reaction/2426027
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2,3,4-Tetrahydro-1-naphthylamine | HCID 18066 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,4-Difluoro-1-(methylsulfonyl)benzene | HCID 2758336 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11551484 | HCID 11551484 | 114.7% |
Reaction Steps
A solution of 1,2,3,4-tetrahydronaphthalen-1-amine (0.82 mL, 5.73 mmol), 2,4-difluoro-1-(methylsulfonyl)benzene (1.1 g, 5.73 mmol) and diisopropylethylamine (2.0 mL, 11.46 mmol) in CH3CN (15 mL) was stirred at 60° C. for 48 h. The solvent was concentrated in vacuo, the residue was taken up in dichloromethane and washed with water and brine, dried, and concentrated under reduced pressure to yield 2.1 g of a yellow oil. The residue was purified by PTLC (20% ethyl acetate in hexanes) to give 720 mg (39%) of the desired aniline: 1H NMR (400 MHz, CDCl3) δ 7.78 (dd, 1H), 7.28-7.13 (m, 3H), 6.60 (dd, 1H), 6.51-6.45 (m, 2H), 4.62 (dd, 1H), 2.96 (s, 3H), 2.91-2.74 (m, 2H), 2.05-1.98 (m, 2H), 1.91-1.85 (m, 2H). MS (ESI) m/z: Calculated: 319.39; Observed: 661.0 (2M++23).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968538B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-4dfb71f189ee40daa9ef9f763ec38b5b |
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| Source note | uspto-grants-2011_06 |
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