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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014920Generated: October 31, 2026

Boron trifluoride etherate → HCID 66671642, compound

https://huagongshe.com/reaction/1014920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantHCID 86617953HCID 86617953—
SolventDichloromethaneHCID 6344—
ProductHCID 66671642HCID 6667164251%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution containing crude 61 (16.7 g, 0.059 mol) in DCM (150 mL) was cooled to −78° C. BF3.Et2O (8.9 mL, 0.07 mol) was added followed by the dropwise addition of DIBAL (2 M/DCM, 200 mL, 0.4 mol). After 2 h, TLC analysis indicated complete consumption of the 61 [TLC analysis: 1:1 hexane/EtOAc, Rf(62)=0.3]. EtOAc (40 mL) was added and the reaction mixture was warmed to −15° C. The reaction mixture was carefully quenched with 1M HCl until pH=2. The product was extracted with DCM. The organic extracts were washed with 1M HCl, water, and brine, dried over anhydrous Na2SO4, filtered, and concentrated. The crude 62 was purified by silica gel chromatography (2:1 hexanes/EtOAc) to afford 7.2 g (51%) of 62. 1H NMR (CDCl3, 300 MHz) δ5.8-5.5 (m, 2H), 4.18 (m, 2H), 4.0-3.25 (m, 3H), 2.2-1.85 (m, 2H), 1.55-1.3 (m. 1H), 1.43 (s, 9H), 1.15 (d, J=6 Hz, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985735B2
Source datasetuspto-grants-2011_07
ORD IDord-97d455a1d0f04acca4349234b3e978cc
Source noteuspto-grants-2011_07