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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479808Generated: October 30, 2026

Water → (4-Benzyl-1,4-oxazepan-2-ylmethyl)-phenyl amine

https://huagongshe.com/reaction/479808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium IodideHCID 5238—
ReactantAnilineHCID 6115—
Reactant4-Benzyl-2-(chloromethyl)-1,4-oxazepaneHCID 10399365—
Solvent1-ButanolHCID 263—
SolventDichloromethaneHCID 6344—
Product(4-Benzyl-1,4-oxazepan-2-ylmethyl)-phenyl amineHCID 21904409—

Reaction Conditions

Temperature110 °C

Reaction Steps

Aniline (2.59 mL, 28.4 mmol) and NaI (4.06 g, 27.1 mmol) were added to a solution of 4-benzyl-2-chloromethyl-1,4-oxazepane (79) (6.49 g, 27.1 mmol) in n-butanol (68 mL, 0.4 M), and the reaction was heated to 110° C. until the reaction was judged complete by TLC (4 h). The reaction was cooled to room temperature, and water and CH2Cl2 were added. The organic layer was removed, and the aqueous layer was extracted with CH2Cl2 (2×). The combined organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo to achieve (4-benzyl-1,4-oxazepan-2-ylmethyl)-phenyl amine 80, which was used without purification in the next reaction. 1H NMR (partial, CDCl3) 4.08-3.86 (3H, m), 3.80 (1H, d, J=13.3 Hz), 3.73 (1H, d, J=13.3 Hz), 3.22-3.05 (2H, m), 2.95-2.70 (3H, m), 2.64 (1H, dd, J=13.6, 7.6 Hz), 2.1-1.9 (2H, m) ppm. 13C NMR (CDCl3) 148.33, 139.38, 129.28, 129.11, 128.46, 127.23, 117.44, 113.13, 76.70, 67.49, 62.92, 59.35, 54.76, 46.93, 30.75 ppm. LRMS: 296.68.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06645980B1
Source datasetuspto-grants-2003_11
ORD IDord-a7d04b699be94bb4a7df58dbfb380e88
Source noteuspto-grants-2003_11