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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188985Generated: October 30, 2026

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

https://huagongshe.com/reaction/2188985

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 numberUS08324223B2
Source datasetuspto-grants-2012_12
ORD IDord-65595a8452f1445c97512c1fb5e7b9fb
Source noteuspto-grants-2012_12