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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885947Generated: October 31, 2026

Triethylamine → 2-(6-Chloropyridin-3-yl)ethan-1-ol

https://huagongshe.com/reaction/885947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(6-Chloropyridin-3-yl)acetic acidHCID 14071571—
SolventTetrahydrofuranHCID 8028—
Product2-(6-Chloropyridin-3-yl)ethan-1-olHCID 14071572110.4%

Reaction Steps

To a stirred solution of 2-chloropyridine-5-acetic acid (800 mg, 4.60 mmol) in THF (30 mL) at 0° C. under a nitrogen atmosphere was added triethylamine (2.20 mL, 10.3 mmol) and isobutyl chloroformate (1.20 mL, 9.33 mmol). The reaction was stirred for 50 minutes then sodium borohydride (1.77 g, 46 mmol) was added and the suspension stirred at r.t. for 16 h then at reflux for a further 4 h. The resulting mixture was partitioned between DCM (50 mL) and water (50 mL). The organic fraction was washed with brine (50 mL), dried (MgSO4) and concentrated in vacuo to yield the title compound (800 mg, quantitative) as a brown oil. LCMS (ES+) 158.0 (M+H)+, RT 1.81 minutes (85% purity) (Method 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242116B2
Source datasetuspto-grants-2012_08
ORD IDord-bfc67cf8fb004e7fb6bc63fe35a030db
Source noteuspto-grants-2012_08