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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725726Generated: November 3, 2026

Triethylamine → HCID 67301514, compound

https://huagongshe.com/reaction/1725726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butyl methyl etherHCID 15413—
ReactantHCID 67301556HCID 67301556—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67301514HCID 67301514—

Reaction Steps

12.3 g (54.4 mmol) 3-(4-chloro-3,5-dimethyl-phenyl)-2-oxo-propionic acid in 130 mL THF and 7.6 mL (54.4 mmol) triethylamine were combined at -35° C. with a solution of 21.0 g (65.3 mmol) (1R)-B-chlorodiisopinocampheylborane in 65 mL THF within 30 min and stirred for 2 h at this temperature. After the reaction had ended the reaction mixture was made alkaline at 0° C. with 50 mL 1 M NaOH (exothermic), stirred for 3 h, combined with 30 mL TBME and the phases were separated. The organic phase was washed with 50 mL water and 30 mL 1 M NaOH. The combined aqueous phases were acidified with 2 M HCl and extracted with TBME. The organic phases were dried over Na2SO4 and evaporated down i. vac. The product was reacted further without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491717B2
Source datasetuspto-grants-2009_02
ORD IDord-4eb7cd0c1dab475ba19a422a7ff61aaf
Source noteuspto-grants-2009_02