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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426050Generated: November 1, 2026

Diisopropylethylamine → HCID 58707278, compound

https://huagongshe.com/reaction/2426050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4-Difluoro-1-(methylsulfonyl)benzeneHCID 2758336—
Reactant3,4-Dihydro-2H-1-benzopyran-4-amineHCID 4961957—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 58707278HCID 5870727858.6%

Reaction Steps

A solution of chroman-4-amine (0.38 g, 2.55 mmol), 2,4-difluoro-1-(methylsulfonyl)benzene (0.49 g, 2.55 mmol) and diisopropylethylamine (2.2 mL, 12.74 mmol) in N,N-dimethylformamide (10 mL) was stirred at 90° C. for 16 h. The reaction mixture was diluted with water and extracted with diethyl ether. The combined extracts were washed with water and brine, dried, and concentrated under reduced pressure to yield 0.48 g of a yellow oil. The residue was purified by PTLC (25% ethyl acetate in hexanes) to give 0.45 g (55%) of the desired aniline: 1H NMR (400 MHz, CDCl3) δ 7.62 (dd, 1H), 7.35 (d, 1H), 7.28 (m, 1H), 6.91 (m, 1H), 6.85 (d, 1H), 6.57 (dd, 1H), 6.42 (dd, 1H), 4.49 (m, 1H), 4.34 (bs s, 1H), 4.29 (m, 2H), 2.86 (s, 3H), 2.23 (m, 2H). MS (ESI) m/z: Calculated: 321.08; Observed: 322.2 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968538B2
Source datasetuspto-grants-2011_06
ORD IDord-02d22453275043848862b264d41e4b80
Source noteuspto-grants-2011_06