Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259804Generated: October 31, 2026

4-Phenoxybenzaldehyde → HCID 59263537, compound

https://huagongshe.com/reaction/1259804

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenoxybenzaldehydeHCID 66139—
ReactantCyclopropanemethanamineHCID 75646—
ReactantTriacetoxyborohydrideHCID 2724942—
ReactantHCID 86609017HCID 86609017—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59263537HCID 5926353763.7%

Reaction Steps

To a solution of 3-(2′-oxospiro[furo[2,3-f][1,3]benzodioxole-7,3′-indol]-1′(2′H)-yl)propanal (0.07 g, 0.20 mmol) in THF (5.00 mL) was added (aminomethyl)cyclopropane (0.30 mmol) and MP-triacetoxyborohydride (0.26 g, 0.60 mmol). After overnight shaking, the polymer-bound 4-phenyloxybenzaldehyde (0.25 g, 0.18 mmol) was added. After another overnight shaking, the mixture was diluted with ether (10.0 mL) and filtered. The filtrate was concentrated in vacuo to dryness. The residue was recrystallized to give the title compound (0.05 g) in 62% yield as a white solid: 1H NMR (300 MHz, CDCl3) δ 7.32-6.92 (m, 4H), 6.49 (s, 1H), 6.12 (s, 1H), 5.83 (m, 2H), 4.86 (m, 1H), 4.64 (m, 1H), 3.97-3.77 (m, 2H), 2.87-2.80 (m, 2H), 2.66-2.56 (m, 2H), 1.02-0.94 (m, 1H), 0.56-0.47 (m, 2H), 0.25-0.18 (m, 2H); MS (ES+) m/z 393.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466188B2
Source datasetuspto-grants-2013_06
ORD IDord-00f986a28b134d1799c0cd1c61001050
Source noteuspto-grants-2013_06