참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | N-[(1,1-Dimethylethoxy)carbonyl]glycine-4phenylmethoxy-2-butenyl ester | HCID 69891095 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 촉매 | Zincchloride | HCID 3007855 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 2-[(1,1-Dimethylethoxy)carbonyl]amino-3-phenylmethoxy-4pentenoic acid | HCID 23508263 | — |
반응 단계
A lithium diisopropylamide solution (37.3 M) is prepared from N,N-diisopropylamine (5.2 mL, 37.2 mmol) in THF (30 mL. cooled to −20° C.) and 3.7 mL (37.3 mmol) 10 M n-BuLi in hexane. The LDA solution in THF is added to a stirred solution of N-[(1,1-dimethylethoxy)carbonyl]glycine-4-phenylmethoxy-2-butenyl ester 63a (14.9 mmol) and ZnCl2 (17.9 mmol) in 100 mL THF at −78° C. The mixture is allowed to come to room temperature overnight. The crude mixture is partitioned between 700 mL ethyl acetate and 700 mL 1 N HCl. The organic layer is washed with 150 mL dilute NaHCO3 solution (3×'s). The bicarbonate washes are acidified with conc. HCl to pH1 and extracted with 700 mL ethyl acetate. The ethyl acetate layer is dried over magnesium sulfate and the solvent removed in vacuo to give the named compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06566381B1 |
|---|
| 출처 데이터셋 | uspto-grants-2003_05 |
|---|
| ORD ID | ord-6de3ff56f63c420ca8f09f42aad1a704 |
|---|
| 출처 메모 | uspto-grants-2003_05 |
|---|