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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2385244Generated: October 30, 2026

5,6-dihydro-2H-spiro[benzofuro[6,5-b]furan-3,3'-indolin]-2'-one → HCID 59352643, compound

https://huagongshe.com/reaction/2385244

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,6-dihydro-2H-spiro[benzofuro[6,5-b]furan-3,3'-indolin]-2'-oneHCID 59263354—
Reactant6-Methoxy-5-methylspiro[1-benzofuran-3,3'-indol]-2'(1'H)-oneHCID 59352225—
ProductHCID 59352643HCID 59352643—

Reaction Steps

Following the procedure as described in EXAMPLE 4 and making non-critical variations using 6-methoxy-5-methylspiro[1-benzofuran-3,3′-indol]-2′(1′H)-one to replace 5,6-dihydrospiro[benzo[1,2-b:5,4-b′]difuran-3,3′-indol]-2′(1′H)-one, 6-methoxy-5-methyl-1′-(tetrahydro-2H-pyran-2-ylmethyl)spiro[1-benzofuran-3,3′-indol]-2′(1′H)-one was obtained (68%) as a colorless solid: mp 180-182° C.; 1H NMR (300 MHz, CDCl3) δ 7.28 (dd, J=7.8, 7.8 Hz, 1H), 7.13-6.97 (m, 3H), 6.47 (s, 1H), 6.43 (d, J=4.3 Hz, 1H), 4.91 (dd, J=8.9, 2.1 Hz, 1H), 4.66 (dd, J=8.9, 3.3 Hz, 1H), 4.02-3.59 (m, 4H), 3.79 (s, 3H), 3.43-3.31 (m, 1H), 1.99 (s, 3H), 1.92-1.77 (m, 1H), 1.71-1.26 (m, 5H); MS (ES+) m/z 380.4 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263606B2
Source datasetuspto-grants-2012_09
ORD IDord-5a299772b1a241a2afe195f5d398f8c7
Source noteuspto-grants-2012_09