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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422511Generated: November 3, 2026

1,3-Thiazole-2-carbaldehyde → HCID 59774862, compound

https://huagongshe.com/reaction/2422511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Thiazole-2-carbaldehydeHCID 2734903—
Reactant3-(methoxymethoxy)tolueneHCID 10964701—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59774862HCID 59774862—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) solution of t-BuLi (1.7 M in pentane, 5.0 mL, 8.5 mmol), 1-(methoxymethoxy)-3-methylbenzene (see example 33, step 1) was added dropwise (1.18 g, 7.73 mmol), maintaining the internal temperature below 16° C. The suspension was stirred at 0° C. for 1 h, cooled to −78° C., and THF (15 mL) was added. A solution of 1,3-thiazole-2-carboxaldehyde (0.962 g, 8.5 mmol) was added and the cooling bath was removed. The reaction mixture was allowed to warm to 0° C., extracted twice with EtOAc from NH4Cl, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography (30-50% EtOAc in hexanes) to afford the title compound. 1H NMR (400 MHz, acetone-d6): 7.77 (d, 1H), 7.48 (s, 1H), 7.33 (d, 1H), 6.95 (s, 1H), 6.83 (d, 1H), 6.36 (d, 1H), 5.32 (d, 1H), 5.21 (s, 2H), 3.38 (s, 3H), 2.32 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960409B2
Source datasetuspto-grants-2011_06
ORD IDord-3c8412b9ceec40f3bc372a029dc07bee
Source noteuspto-grants-2011_06