Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205520Generated: November 1, 2026

Diethyl Ether → HCID 86680489, compound

https://huagongshe.com/reaction/2205520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantHCID 86680488HCID 86680488—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86680489HCID 8668048963%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-(1H-pyrazol-4-yl)thiazole-5-carbaldehyde (245 mg, 1.3 mmol) in THF (15 mL) was cooled to 0° C., a 3M solution of ethyl magnesium bromide in diethyl ether (0.9 mL, 2.7 mmol) slowly added at 0° C., and the reaction mixture stirred for 2 hours at 0° C. The reaction mixture was quenched with saturated NH4Cl solution (10 mL) and extracted with ethyl acetate (2×200 mL). The combined extracts were washed with brine solution (20 mL), dried over Na2SO4, filtered and the organic solvent was concentrated under reduced pressure to obtain crude product. The crude product was purified by flash chromatography (60-120μ; 3% methanol in dichloromethane) to afford 1-(2-(1H-pyrazol-4-yl)thiazol-5-yl)propan-1-ol as pale yellow liquid (180 mg, 63% yield). 1H NMR (400 MHz, DMSO-d6): δ 13.19 (br s, 1H), 8.25 (s, 1H), 7.88 (s, 1H), 7.51 (s, 1H), 5.59 (d, 1H), 4.71 (q, 1H), 1.97-1.64 (m, 2H), 0.86 (t, 3H); LC-MS m/z calculated for [M+H]+210.06. found 210.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371316B2
Source datasetuspto-grants-2016_06
ORD IDord-f158f96c183d427d984fad38d5ac3f1d
Source noteuspto-grants-2016_06