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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746051Generated: November 2, 2026

Ammonium Chloride → HCID 90414084, compound

https://huagongshe.com/reaction/1746051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
ReactantHCID 12946522HCID 12946522—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90414084HCID 90414084—

Reaction Conditions

Temperature-70 °C

Reaction Steps

5-Bromobenzo[d][1,3]oxathiole (1.0 g, 4.6 mmol, prepared as described in Cabiddu, Salvatore; Cerioni, Giovanni; Cocco, Maria Teresa; Maccioni, Antonio; Plumitallo, Antonio, Journal of Heterocyclic Chemistry 1982, 19, 135-139) was dissolved in dry tetrahydrofuran (12 mL), cooled to −70° C., treated in portions with n-BuLi (2.5 M; 1.9 mL, 4.8 mmol) and stirred at −70° C. for 30 min. 4,4,5,5-Tetramethyl-1,3,2-dioxaborolane (900 mg, 4.8 mmol) was added and stirring was continued for 1.5 h during which the temperature rose to −30° C. The mixture was treated with saturated NH4Cl (5 mL) and extracted with ethyl acetate (2×25 mL). The combined extracts were washed with saturated NaCl (10 mL), dried (Na2SO4) and evaporated to give the title compound which was used without further purification (1.2 g, 99%): 1H NMR (400 MHz, CDCl3) δ 7.62 (d, J=1.1 Hz, 1H), 7.48 (dd, J=8.0, 1.3 Hz, 1H), 6.82 (d, J=8.1 Hz, 1H), 5.69 (s, 2H), 1.32 (s, 12H); EIMS m/z 264.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149038B2
Source datasetuspto-grants-2015_10
ORD IDord-05f91508ad484bac909b14f77b2fdb07
Source noteuspto-grants-2015_10