참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 반응물 | Methyl 4-[(4-methylbenzenesulfonyl)oxy]benzoate | HCID 1771995 | — |
| 반응물 | HCID 178444609 | HCID 178444609 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | Benzoic acid, 4-hexyl-, methyl ester | HCID 591633 | 83% |
반응 단계
A flame-dried two-necked flask is charged under argon with 4-(4-methylbenzenesulfonyloxy)benzoic acid methyl ester (0.50 g, 1.63 mmol), Fe(acac)3 (29 mg, 0.08 mmol), THF (10 mL) and N-methylpyrrolidone (NMP, 0.95 mL). A solution of n-hexylmagnesium bromide (2M in Et2O, 1 mL, 2 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 (298 mg, 83%). 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-2ba5223bac5c431aa435d0edd11aabad |
|---|
| 출처 메모 | uspto-grants-2006_04 |
|---|