HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4,6-Trimethylphenol → HCID 57848879, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4,6-Trimethylphenol | HCID 10698 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,4-Dichlorothieno[3,2-d]pyrimidine | HCID 12712832 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57848879 | HCID 57848879 | 56% |
Reaction Steps
A stirred suspension of NaH (7.8 mg, 0.19 mmol) in dry THF (1 mL) was added 2,4,6-trimethyl phenol (26.4 mg, 0.19 mmol) and stirred at room temperature for 30 min under Argon. The reaction mixture was added to a solution of 2,4-dichlorothieno[3,2-d]pyrimidine (39.6 mg, 0.19 mmol) in dry THF (1 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 (32.4 mg, 56%):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595324B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-b535adf7dadd46bd86c6db15df247f34 |
| Source note | uspto-grants-2009_09 |