참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 1-Boc-D-Pyroglutamic acid ethyl ester | HCID 820885 | — |
| 반응물 | HCID 178478191 | HCID 178478191 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | ethyl (R)-2-tert-butoxycarbonylamino-5-(4-chlorophenyl)-5-oxopentanoate | HCID 67371186 | — |
반응 단계
To a solution of (R)-5-oxopyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester (CAS No. 128811-48-3; 4.0 g) in tetrahydrofuran (100 mL), 4-chlorophenylmagnesium bromide (1.0 M solution in diethyl ether; 17.1 mL) was added dropwise at −40° C. over 20 minutes, and the reaction solution was stirred at −40° C. to 0° C. for one hour. Water was added to the solution in small portions at 0° C., followed by extraction with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (heptane-ethyl acetate system) to obtain 5.6 g of the title compound as a colorless oil. The property values of the compound are as follows.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08048878B2 |
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| 출처 데이터셋 | uspto-grants-2011_11 |
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| ORD ID | ord-3a471e17106143ac9a3ff2b3fe3745ff |
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| 출처 메모 | uspto-grants-2011_11 |
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