참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 반응물 | Methyl 4-(((trifluoromethyl)sulfonyl)oxy)benzoate | HCID 5315090 | — |
| 반응물 | HCID 178444609 | HCID 178444609 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | Benzoic acid, 4-hexyl-, methyl ester | HCID 591633 | 93% |
반응 단계
A flame-dried two-necked flask is charged under argon with 4-(trifluoromethylsulfonyloxy)benzoic acid methyl ester (760 mg, 2.66 mmol), Fe(acac)3 (47 mg, 0.13 mmol), THF (30 mL) and N-methylpyrrolidone (NMP, 1.7 mL). A solution of n-hexylmagnesium bromide (2M in Et2O, 1.7 mL, 3.4 mmol) is added via syringe to the resulting red solution, causing an immediate color change to dark brown and finally to violet. The resulting mixture is stirred for 5 min, the reaction is diluted with Et2O and is carefully quenched upon addition of aq. HCl (1M, ca. 10 mL). Work-up followed by flash chromatography of the crude product as described above provides 4-hexylbenzoic acid methyl ester as a colorless syrup (540 mg, 93%). The spectroscopic and analytical data are identical to those compiled above.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07026478B2 |
|---|
| 출처 데이터셋 | uspto-grants-2006_04 |
|---|
| ORD ID | ord-247077bc74b74d10a2c4b0718a7f4454 |
|---|
| 출처 메모 | uspto-grants-2006_04 |
|---|