HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723486Generated: October 30, 2026
Lithium borohydride → HCID 66952775, compound
https://huagongshe.com/reaction/723486
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 66953071 | HCID 66953071 | — |
| Product | HCID 66952775 | HCID 66952775 | — |
Reaction Steps
To a solution of 261B (270 mg, 0.75 mmol) was added LiBH4 (15.5 mg, 0.71 mmol). The mixture was heated to reflux for 1.0 hr. HPLC showed still some starting material remaining. More LiBH4 (15.5 mg, 0.71 mmol) was added, and the mixture was heated for another 2.0 hrs. After cooling to room temperature, ice water was added, and the mixture was concentrated in vacuo to remove the THF. The aqueous residue was extracted with EtOAc (×3) and the combined extracts were dried (Na2SO4), and concentrated in vacuo. The residue was taken into 2 mL of CH2Cl2 and 2 mL of TFA was added. The mixture was stirred at room temperature for 30 min. The mixture was concentrated in vacuo, followed by drying under high vacuum overnight to afford 261C as an oil. It had an analytical HPLC retention time=0.590 min. (Chromolith SpeedROD column 4.5×50 mm, 10–90% aqueous methanol containing 0.1% TFA over 4 min, 4 mL/min, monitoring at 220 nm) and a LC/MS M++1=235. This material was used directly in the next reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141571B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-3043efa3bd984ad585f06761975bec60 |
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| Source note | uspto-grants-2006_11 |
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