HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660701Generated: October 31, 2026
Potassium borohydride → HCID 11242828, compound
https://huagongshe.com/reaction/1660701
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium borohydride | HCID 4192641 | — |
| Reactant | HCID 11231121 | HCID 11231121 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11242828 | HCID 11242828 | — |
Reaction Steps
To a solution of methyl ester 45 (2.4 g, 8.70 mmol) in HPLC MeOH (100 mL), cooled to −78° C., potassium borohydride (1.4 g, 26.1 mmol) was added in portions. The reaction mixture was stirred at −78° C. for 10 min, warmed to −20° C. for 30 min and then to 0° C. for 10 min. The reaction was quenched with acetic acid to pH=7 and extracted with CH2Cl2 (3×50 mL). The organic layer was washed with NaHCO3 (50 mL, sat), NaCl (50 mL, sat), dried (Na2SO4), filtered, and evaporated. The alcohol 46 was obtained as a colorless oil (2.2 g, 92%) and used directly in the next step. 1H-NMR (500 MHz, CDCl3): 0.88 (d, J=6.8 Hz, 3H), 0.93 (d, J=6.8 Hz, 3H), 1.44 (s, 9H), 2.03-2.17 (m, 1H), 2.41-2.52 (m, 1H), 2.58-2.63 (m, 1H), 3.50-3.55 (m, 1H), 3.71 (s, 3H), 3.89-3.93 (m, 1H), 3.38-3.41 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030279B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-b527e6c09a0b4d30ac47c25a6b1b6954 |
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| Source note | uspto-grants-2011_10 |
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