Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024546Generated: November 1, 2026

Hydrochloric Acid → HCID 86670078, compound

https://huagongshe.com/reaction/1024546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 60172445HCID 60172445—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 86670078HCID 86670078—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a suitable reactor was added 3g (1.19 g, 1.0 equiv) and EtOH (6 mL) was added at 20-30° C. under N2. The mixture was cooled to −25 to −15° C., and NaBH4 (107.1 mg, 0.8 equiv) in H2O (2.4 mL) was added at below −15° C. The reaction mixture was warmed to −5-5° C. and stirred for 1 hr. The reaction was deemed completed as determined by TLC. 1N HCl aqueous solution (11 mL) was added at below 10° C., and the mixture was warmed to 20-30° C. EtOAc (100 mL) was added at 20-30° C., and the mixture was stirred at this temperature for 30 min. The separated organic portion was concentrated under reduced pressure to afford crude 4g. The diastereomeric ratio of crude 4g was determined to be 95/5 by HPLC analysis. The residue was purified by flash column chromatography (EtOAc/n-heptane=1/1) to give a diastereomeric mixture of 4g (0.84 g, 82% yield) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722921B2
Source datasetuspto-grants-2014_05
ORD IDord-8f62a8db36b84d12985db536e45891ad
Source noteuspto-grants-2014_05