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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902778Generated: October 31, 2026

Water → HCID 11611418, compound

https://huagongshe.com/reaction/902778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 4289537HCID 4289537—
Reactant6-Amino-2,2-dimethyl-benzo[1,3]dioxin-4-oneHCID 11615330—
SolventTolueneHCID 1140—
ProductHCID 11611418HCID 11611418105.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-formylbenzoate (481 mg) and 6-amino-2,2-dimethyl-4H-1,3-benzodioxin-4-one (386 mg) in toluene (20 mL) was heated at reflux for 12 h with azeotropic removal of water. The toluene was evaporated off under reduce pressure, the residue was taken up in methanol (10 mL) and cooled to 0° C. NaBH4 (114 mg) was added portionwise and the reaction mixture was stirred at 0° C. for 1 h then at rt for 2 h. The reaction mixture was poured into water and resulting mixture extracted with Et2O. The combined organic layers were washed with brine, dried over MgSO4 and filtered. The solvent was removed under reduce pressure to give the crude product as an oil. The product was purified by flash chromatography (SiO2, EtOAc/c-Hex 20/80) to give the title compound as a colorless oil (713 mg, 85%). 1H NMR (CDCl3) δ 8.07 (d, J=8.1 Hz, 2H), 7.54-7.32 (m, 7H), 7.17 (d, J=2.6 Hz, 1H), 6.89-6.78 (m, 2H), 5.37 (s, 2H), 4.41 (s, 2H), 1.70 (s, 6H). M+(ESI): 418.3; M−(ESI): 416.1. HPLC, Rt: 4.6 min (purity: 95.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365225B2
Source datasetuspto-grants-2008_04
ORD IDord-c64b4e056a6c47c9a5dc47981468a152
Source noteuspto-grants-2008_04