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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746059Generated: November 1, 2026

Hydrochloric Acid → HCID 90413889, compound

https://huagongshe.com/reaction/1746059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5017741—
ReactantHCID 90413453HCID 90413453—
SolventSodium ChlorideHCID 5234—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 90413889HCID 90413889—

Reaction Conditions

Temperature-2.5 °C

Reaction Steps

6-Bromo-2,2,4-trifluorobenzo[d][1,3]dioxole (2.0 g, 7.8 mmol) was dissolved in dry tetrahydrofuran (10 mL), cooled to −5 to 0° C. and treated in portions with isopropylmagnesium lithium chloride complex (1.3 M; 6.3 mL, 8.2 mmol). The cooling bath was removed and the mixture was stirred for 30 min. 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.6 g, 8.4 mmol) was added, the mixture was stirred for 1 h and then treated with saturated NH4Cl (5 mL). The mixture was diluted with ethyl acetate (40 mL) and saturated NaCl (10 mL) and the pH was adjusted to 2 by addition of HCl. The organic phase was washed with saturated NaCl (5 mL), dried (Na2SO4) and evaporated to give the title compound which was used without further purification (2 g, 85%): 1H NMR (400 MHz, CDCl3) δ 7.36 (d, J=9.8 Hz, 1H), 7.29 (d, J=6.5 Hz, 1H), 1.33 (s, 12H); 19F NMR (376 MHz, CDCl3) δ −49.79, −136.26; EIMS m/z 302.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149038B2
Source datasetuspto-grants-2015_10
ORD IDord-3ad8b0ce49314aceb6db00e48b2c80ce
Source noteuspto-grants-2015_10