Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Trimethyl borate → 3-(1-Methyl-3-pentylureido)phenylboronic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Trimethyl borate | HCID 8470 | — |
| 반응물 | 1-(3-Bromophenyl)-1-methyl-3-pentylurea | HCID 67272794 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 반응물 | HCID 178418348 | HCID 178418348 | — |
| 용매 | Pentane | HCID 8003 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-(1-Methyl-3-pentylureido)phenylboronic acid | HCID 67273272 | 39% |
반응 단계
In a manner similar to that of Example (18a), by reaction of 123 g (0.411 mol, 1 eq) of 1-(3-bromophenyl)-1-methyl-3-pentylurea in 1.23 L of tetrahydrofuran, 150 mL (0.452 mol, 1.1 eq) of methyllithium, 530 mL (0.904 mol, 2.2 eq) of a 1.7 M solution of tert-butyllithium in pentane and 115 mL (0.904 mol, 2.2 eq) of trimethyl borate, and after purification by chromatography on silica gel (50/50 heptane/ethyl acetate) and crystallization from ethyl acetate/heptane, 42.0 g of 3-(1-methyl-3-pentylureido)phenylboronic acid are obtained in the form of a pink-colored powder. Yield=39%
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07863332B2 |
| 출처 데이터셋 | uspto-grants-2011_01 |
| ORD ID | ord-b51e54c96bc14c959fc6dba60834ce53 |
| 출처 메모 | uspto-grants-2011_01 |