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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731110Generated: October 31, 2026

Dichloromethane → HCID 68814892, compound

https://huagongshe.com/reaction/731110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 68815678HCID 68815678—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68814892HCID 68814892—

Reaction Steps

The desired product was prepared using a procedure similar to step 3 of example 3. Thus, 3-benzyl-5-bromo-1-methyl-2-phenyl-1H-indole (1.525 g, 4.053 mmol) was reacted with aqueous 2M K2CO3 (4.1 ml), 4-methoxyphenylboronic acid (0.862 g, 5.674 mmol) [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II) complex with dichloromethane (1:1) (0.099 g, 0.122 mmol) in dioxane (41 ml) to give the product (0.766 g, 1.898 mmol, 47%) as an off-white solid, mp 122-125° C. 1H NMR (DMSO-d6) δ 3.62 (s, 3H), 3.77 (s, 3H), 4.04 (s, 2H), 6.98 (d, J=8.6 Hz, 2H), 7.07-7.11 (m, 3H), 7.18 (t, J=7.8 Hz, 2H), 7.42 (dd, J=1.5, 8.6 Hz, 1H), 7.45-7.55 (m, 9H); [ESI(+)], m/z 405 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582773B2
Source datasetuspto-grants-2009_09
ORD IDord-7f5f7a07f26a4733a7835ef6fc05aee3
Source noteuspto-grants-2009_09