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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736316Generated: October 29, 2026

2,4,6-Trimethylphenol → 2-Chloro-4-(mesityloxy)thieno[2,3-d]pyrimidine

https://huagongshe.com/reaction/736316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylphenolHCID 10698—
ReactantSodium hydrideHCID 24758—
Reactant2,4-Dichlorothieno[2,3-d]pyrimidineHCID 12217324—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-4-(mesityloxy)thieno[2,3-d]pyrimidineHCID 5784887797.1%

Reaction Steps

A stirred suspension of NaH (9.5 mg, 0.24 mmol) in dry THF (1 mL) was added 2,4,6-trimethyl phenol (32.1 mg, 0.24 mmol) and stirred at room temperature for 30 min under Argon. The reaction mixture was added to a solution of 2,4-dichlorothieno[2,3-d]pyrimidine (48.1 mg, 0.24 mmol) in dry THF (1.5 mL) at 0° C. and allow it to slowly warmed up to room temperature. After stirring the reaction for 4 h, the resulting mixture was diluted with water and washed with EtOAc. The combined organic layers were washed with water, brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (9:1) to give the product as a white solid (71 mg, 97%):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595324B2
Source datasetuspto-grants-2009_09
ORD IDord-48842ee22dfe41f58839d6f4ce79cbb3
Source noteuspto-grants-2009_09