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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423407Generated: October 29, 2026

Acetic Acid → HCID 66674145, compound

https://huagongshe.com/reaction/423407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 53629854HCID 53629854—
SolventMethanolHCID 887—
ProductHCID 66674145HCID 6667414556.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolve (R)-1-(5-bromo-pyridin-2-yl)-pyrrolidin-3-ylamine (1.60 g, 6.63 mmol) in CH3OH (915 mL). Add (1-ethoxy-cyclopropoxy)-trimethyl-silane (2.7 mL, 13.49 mmol) and HOAc (1.9 mL, 33.15 mmol) and stir at RT for 3 h. Add NaBH3CN (4.2 g, 66.30 mmol) and reflux overnight. Cool the mixture to 0° C., quench with 2.0 M NaOH (15 mL), and dilute with H2O (100 mL). Extract with EtOAc (3×100 mL). Wash the combined organic layers with 1.0 M NaOH (50 mL), H2O (100 mL), and brine (50 mL). Dry the solution with Na2SO4, filter, and concentrate. Purify the crude material by chromatography, eluting with 0.5% Et3N, 5% CH3OH and 95% CHCl3 to give 1.20 g (56%) of the title compound. MS/ES m/z (79Br) 322 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101764B2
Source datasetuspto-grants-2012_01
ORD IDord-38f2f760ba0b4edfb0065174a5ca6a2a
Source noteuspto-grants-2012_01