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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660701Generated: October 31, 2026

Potassium borohydride → HCID 11242828, compound

https://huagongshe.com/reaction/1660701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium borohydrideHCID 4192641—
ReactantHCID 11231121HCID 11231121—
SolventMethanolHCID 887—
ProductHCID 11242828HCID 11242828—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030279B2
Source datasetuspto-grants-2011_10
ORD IDord-b527e6c09a0b4d30ac47c25a6b1b6954
Source noteuspto-grants-2011_10