HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014920Generated: October 31, 2026
Boron trifluoride etherate → HCID 66671642, compound
https://huagongshe.com/reaction/1014920
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | HCID 86617953 | HCID 86617953 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66671642 | HCID 66671642 | 51% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985735B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-97d455a1d0f04acca4349234b3e978cc |
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| Source note | uspto-grants-2011_07 |
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