Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dimethylamine → N-[(1R)-3-(Dimethylamino)-1-(hydroxymethyl)-3-oxopropyl]carbamic acid phenylmethyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dimethylamine | HCID 674 | — |
| 반응물 | Benzyl (S)-(-)-tetrahydro-5-oxo-3-furanylcarbamate | HCID 697922 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-[(1R)-3-(Dimethylamino)-1-(hydroxymethyl)-3-oxopropyl]carbamic acid phenylmethyl ester | HCID 59186705 | 99% |
반응 단계
A solution of 3-(S)-((carbobenzyloxy)amino)-γ-butyrolactone (prepared according to the procedure described in McGarvey, G. J.; Williams, J. M.; Hiner, R. N.; Matsubara, Y.; Oh, T. J. Am. Chem. Soc. 1986, 108, 4943-4952, 7.72 g, 32.8 mmol) in THF (100 mL) was saturated with gaseous dimethylamine, stirred at room temperature for 16 hours, and concentrated. The residue was filtered through a plug of silica gel eluting with 50% acetone in hexanes to give the desired product (9.16 g, 99%). MS (CI) m/e 281 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07585858B2 |
| 출처 데이터셋 | uspto-grants-2009_09 |
| ORD ID | ord-2987bbac10384ccc87a86bdbf15acfb7 |
| 출처 메모 | uspto-grants-2009_09 |