참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Benzenemethanol, 3,5-dichloro-4-hydroxy- | HCID 176409 | — |
| 반응물 | HCID 178418689 | HCID 178418689 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | (Rac.)-2,6-dichloro-4-(1-hydroxyethyl)phenol | HCID 66783703 | 95% |
반응 단계
A sol. of 2,6-dichloro-4-hydroxymethylphenol (1.635 g, 8.56 mmol) in Et2O (30 mL) was cooled to −78° C. MeMgBr (3M in Et2O, 7.15 mL, 21.5 mmol) was added dropwise to the cooled reaction mixture over 18 min. Et2O (20 mL) was added again during the addition of MeMgBr. Stirring was continued at −78° C. for 1 h, and then the reaction mixture was allowed to warm up to rt over 1 h. The mixture was cooled to 0° C., and aq. sat. NH4Cl (10 mL) was added dropwise. The mixture was allowed to warm up to rt, and additional aq. sat. NH4Cl (35 mL) and water (35 mL) were added. The phases were then separated and the aq. phase was extracted with Et2O. The combined org. extracts were then washed with brine (50 mL), dried over MgSO4, filtered, and concentrated under reduced pressure. Purification by FC (EtOAc/heptane, 1:1) yielded the title compound (1.683 g, 95%). LC-MS: tR=0.74 min.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08138340B2 |
|---|
| 출처 데이터셋 | uspto-grants-2012_03 |
|---|
| ORD ID | ord-1323216e7190463894eccacb68d735f7 |
|---|
| 출처 메모 | uspto-grants-2012_03 |
|---|