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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746063Generated: October 31, 2026

Hydrochloric Acid → HCID 90413539, compound

https://huagongshe.com/reaction/1746063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5017741—
ReactantHCID 11195583HCID 11195583—
ReactantCID 53628100HCID 178418400—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90413539HCID 90413539—

Reaction Conditions

Temperature-75 °C

Reaction Steps

(2,2-Difluorobenzo[d][1,3]dioxol-4-yl)trimethylsilane (5.0 g, 22 mmol, prepared as described in Gorecka, Joanna; Leroux, Frederic; Schlosser, Manfred, European Journal of Organic Chemistry 2004, 1, 64-68) was added to a stirred solution of sec-BuLi (1.4 M; 10 mL, 14 mmol) in dry tetrahydrofuran (28 mL) cooled to −75° C. After 2 h at −75° C., 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (4.2 g, 23 mmol) was added, and the mixture was stirred for 90 min at −75° C. The mixture was treated with saturated NH4Cl (5 mL) and warmed to 20° C. The mixture was combined with water (75 mL), acidified with 6 M HCl and extracted with diethyl ether (100 mL). The organic phase was washed with saturated NaCl (15 mL), dried (Na2SO4) and evaporated to give the title compound (estimated purity of 60%) which was used without further purification: 1H NMR (400 MHz, CDCl3) δ 7.39 (d, J=7.5 Hz, 1H), 7.07 (d, J=7.5 Hz, 1H), 1.36 (s, 12H), 0.33 (s, 9H); 19F NMR (376 MHz, CDCl3) δ −49.33; EIMS m/z 356.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149038B2
Source datasetuspto-grants-2015_10
ORD IDord-36f29c1814a24549aeb5191ca88703b9
Source noteuspto-grants-2015_10