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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219194Generated: October 25, 2026

6-Iodoquinolin-3-ol → Tert-butyl 2-(3-hydroxyquinolin-6-yl)acetate

https://huagongshe.com/reaction/219194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Iodoquinolin-3-olHCID 59843085—
ReactantHCID 178451183HCID 178451183—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 2-(3-hydroxyquinolin-6-yl)acetateHCID 57691372—

Reaction Conditions

Temperature75 °C

Reaction Steps

A stirred solution of 6-iodoquinolin-3-ol (1.76 g, 6 mmol) in THF (10 mL) was treated with 2-tert-butoxy-2-oxoethylzinc chloride (39 ml, 19 mmol) followed by tetrakis(triphenylphosphine)palladium(0) (0.8 g, 0.6 mmol). After the addition, it was heated to reflux (75° C.) under N2. After 3 h, TLC 89368-3-1 showed no sign of starting material. Reaction was stop. The reaction was cooled to rt. Solvent was removed. The residue was stirred in EtOAc/10% EDTA (50 mL/50 mL) solution mixture. After 1 h, the organic layer was separated. The aqueous layer was extracted with more EtOAc (2×25 mL). The combined organic layers were washed with water, brine, dried over MgSO4, and removed solvent. The crude product was purified using SiO2 chromatography (TELEDYNE ISCO REDISEP®, PIN 68-2203-026, 12 g sio2, hex:acetone=80%:20%, Flow=30 mL/min). to afford the desired product as brownish liquid. MS m/z: 260.3 (M+H). Calc'd. for C15H17NO3−259.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198448B2
Source datasetuspto-grants-2012_06
ORD IDord-d87bc1b016e94f44bd2baba5ef9c4502
Source noteuspto-grants-2012_06