반응식
Br[CH2:2][C:3]([O:5]C(C)(C)C)=[O:4].[NH:10]1[CH2:14][CH2:13][CH2:12][CH2:11]1.[ClH:15]>C1COCC1.O1CCOCC1>[ClH:15].[N:10]1([CH2:2][C:3]([OH:5])=[O:4])[CH2:14][CH2:13][CH2:12][CH2:11]1참가 물질
6
실험 절차
A solution of 19.6 g (101 mmol) of t-butyl bromoacetate in 150 mL of THF was cooled in an ice bath and treated dropwise over about 0.5 hour with a solution of 14.4 g (202 mmol) of pyrrolidine in 75 mL of THF, to produce a white precipitate. The bath was removed and the reaction slurry stirred for two hours. The solid was removed by filtration and the filtrate was concentrated under reduced pressure to yield a clear liquid over an orange-colored solid. The liquid was cooled in an ice bath, then treated with 40 mL (80 mmol) of 4N HCl in dioxane and stirred for 15 hours. The solvents were removed in vacuo, and the residue was triturated with diethyl ether, then filtered to yield 12.9 g of the desired acid as an off-white solid.
후처리
- customto produce a white precipitate
- customThe bath was removed
- customThe solid was removed by filtration
- concentrationthe filtrate was concentrated under reduced pressure
- customto yield a clear liquid over an orange-colored solid
- temperatureThe liquid was cooled in an ice bath
- stirringstirred for 15 hours
- customThe solvents were removed in vacuo
- customthe residue was triturated with diethyl ether
- filtrationfiltered
출처 및 근거
- ORD 기록
- ord-9cced26fcdcd40c7be9706007486f4b4
- 출처 데이터셋
- uspto-grants-2000_10
- 특허 번호
- US06140505
연결된 노트
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