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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532193Generated: October 31, 2026

Sodium Carbonate → HCID 71571902, compound

https://huagongshe.com/reaction/532193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-Propene, 2-bromo-3,3,3-trifluoro-HCID 272696—
ReactantN,1-dihydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborole-5-carbimidoyl chlorideHCID 86685046—
ReactantHCID 86685066HCID 86685066—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 71571902HCID 715719028%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 2-(3-chloro-4,5-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.2 g, 4.38 mmol), 2-bromo-3,3,3-trifluoroprop-1-ene (920 mg, 5.26 mmol, 1.2 eq), Na2CO3 (1.39 g, 13.14 mmol, 3 eq) and Pd(dppf)Cl2 (358 mg, 10% mol) in DME (50 mL) and water (2 mL) was heated at 70 to 80° C. for 2 h. The mixture was cooled to 0° C. with ice-water bath, and then used to next step without work-up. To the reaction mixture were added TEA (1.33 g, 1.83 mL, 13.14 mmol, 3 eq) and N,1-dihydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborole-5-carbimidoyl chloride (841 mg, 3.50 mmol, 0.8 eq) at 0° C. The reaction mixture was stirred for 12 h at rt, poured into ice-water and extracted with EA. The organic layer was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by silica gel column and prep-HPLC to give 125 mg final title product. 1H NMR (400 MHz, DMSO-d6): δ 9.22 (s, 1 H), 7.76-7.66 (m, 5 H), 4.43 (d, J=18.4 Hz, 1 H), 4.31 (d, J=18.4 Hz, 1 H), 1.48 (s, 6 H) ppm; MS: m/z=444/504 (M−1, ESI−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853186B2
Source datasetuspto-grants-2014_10
ORD IDord-c2dbd2a004284350bd498177e008b731
Source noteuspto-grants-2014_10