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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968752Generated: October 29, 2026

Water → HCID 86583642, compound

https://huagongshe.com/reaction/968752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 86583643HCID 86583643—
CatalystTriphenylphosphineHCID 11776—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 86583642HCID 8658364245.1%

Reaction Steps

5-Bromo-3-cyanomethyl-indole-N-acetic acid, ethyl ester (1.0 g, 3.1 mmol) and phenylboronic acid (0.418 g, 3.4 mmol) were dissolved in anhydrous DME at room temperature under a nitrogen atmosphere and treated with Pd(OAc)2 (2.1 mg, 0.0093 mmol) and PPh3 (7.4 mg, 0.028 mmol). This mixture was heated to reflux and 2 M Na2CO3 (3.11 mL, 6.2 mmol) was added via syringe. After 12 h, the mixture was cooled to room temperature and added to H2O (50 mL). The resultant mixture was extracted with EtoAc (2×, 100 mL) and the organics were combined and washed with a sat'd aqueous NaCl solution, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by SiO2 flash chromatography (heptane to 1:1 heptane/EtOAc) to give the desired material as a white solid (445 mg, 45%); 1H NMR (DMSO-d6, 300 MHz) δ 7.64-7.74 (m, 4H), 7.39-7.44 (m, 4H), 7.29-7.34 (m, 1H), 5.20 (s, 2H), 4.15 (q, J=7.2 Hz, 2H), 4.08 (s, 2H), 1.20 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304079B2
Source datasetuspto-grants-2007_12
ORD IDord-9ee7b82ac7c548a19a796f5bb2d75747
Source noteuspto-grants-2007_12