HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864506Generated: November 2, 2026
Lithium triethylborohydride → HCID 59710338, compound
https://huagongshe.com/reaction/1864506
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium triethylborohydride | HCID 23712863 | — |
| Reactant | HCID 59710219 | HCID 59710219 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59710338 | HCID 59710338 | 74.1% |
Reaction Steps
Superhydride (45.8 mL, 1M, 45.8 mmol) was added dropwise to an ice cold solution of 1,1-dimethylethyl(2R,3S)-3-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-2-{[(methylsulfonyl)oxy]methyl}-1-pyrrolidinecarboxylate (4.69 g, 11.47 mmol) in THF. The reaction was warmed to room temperature and stirred for 16 hours. The reaction was quenched with i-propanol until gas evolution ceased. The reaction was diluted with saturated NaHCO3 then extracted with ethyl acetate, dried over MgSO4 and concentrated under reduced pressure. The crude material was purified by silica gel column chromatography to yield the title compound (2.69 g, 8.5 mmol). 1H NMR (400 MHz, DMSO-D6) δ ppm 0.0 (s, 6H), 0.8 (s, 9H), 1.0 (m, 3H), 1.4 (s, 9H), 1.6 (m, 1H), 2.0 (m, 1H), 3.3 (m, 2H), 3.5 (m, 1H), 4.0 (m, 1H). ES+=316.22.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07625909B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-d99326168f42450cb7838eb173a7e81d |
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| Source note | uspto-grants-2009_12 |
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