HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40300Generated: October 25, 2026
6-Iodoquinolin-3-ol → Tert-butyl 2-(3-hydroxyquinolin-6-yl)acetate
https://huagongshe.com/reaction/40300
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Iodoquinolin-3-ol | HCID 59843085 | — |
| Reactant | HCID 178451183 | HCID 178451183 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 2-(3-hydroxyquinolin-6-yl)acetate | HCID 57691372 | — |
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®, P/N 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524900B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-73f8332e057b4960a4642521c138ba68 |
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| Source note | uspto-grants-2013_09 |
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