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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631059Generated: November 3, 2026

Water → HCID 11301861, compound

https://huagongshe.com/reaction/1631059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Nitrophenylboronic AcidHCID 1677—
ReactantHCID 44478211HCID 44478211—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium CarbonateHCID 10340—
ProductHCID 11301861HCID 11301861—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 5-bromo-2,2,7,8-tetramethyl-chroman-6-ol (400 mg, 1.40 mmol), 3-nitrophenyl boronic acid (300 mg, and Pd(PPh3)4 (100 mg, 5% mol) in glycol dimethyl ether (DME, 20 mL) and 2M Na2CO3 solution (5 mL) was stirred at 120° C. for 3-5 h. After pouring it into water, the mixture was extracted with EtOAc. The EtOAc layer was washed with water, dried and concentrated. The residue was purified by silica gel column chromatography eluting with 10% EtOAc in hexane to give a yellow solid (140 mg). 1H NMR (300 MHz, CDCl3): 8.25-8.16 (μ, 2H), 6.76 (μ, 2H), 4.13 (σ, 1H, OH), 2.27 (μ, 2H), 2.21, 2.19 (2ρ, 6H), 1.68 (μ, 2H), 1.32 (σ, 6H) ppm. 13C NMR (75 MHz, CDCl3) δ: 167.36, 148.79, 145.85, 143.34, 138.27, 136.95, 130.10, 126.51, 125.56, 122.76, 122.29, 115.84, 73.10, 32.83, 27.07, 26.71, 12.95, 12.24, 12.14 ppm. MS: m/z: 328 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791155B2
Source datasetuspto-grants-2014_07
ORD IDord-91f2b545dbf84598a592e9f3629d6c63
Source noteuspto-grants-2014_07