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Sodium borohydride → 6-(1-Hydroxyprop-1-yl)-2-methyl-1,4-benzoxazin-3-(4h)-one

HRID 840367
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인쇄 미리보기

반응식

HRID 840367 반응식
[C:1]([C:5]1[CH:6]=[CH:7][C:8]2[O:13][CH:12]([CH3:14])[C:11](=[O:15])[NH:10][C:9]=2[CH:16]=1)(=[O:4])[CH2:2][CH3:3].[BH4-].[Na+]>C(O)C.C1COCC1>[OH:4][CH:1]([C:5]1[CH:6]=[CH:7][C:8]2[O:13][CH:12]([CH3:14])[C:11](=[O:15])[NH:10][C:9]=2[CH:16]=1)[CH2:2][CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 22623065HCID 22623065, 화합물

생성물 1

HCID 226230436-(1-Hydroxyprop-1-yl)-2-methyl-1,4-benzoxazin-3-(4h)-one수율 95%

시약·촉매·용매 1

HCID 21873804Tetrahydrofuran ethanol용매

실험 절차

6-(Propionyl)-2-methyl-1,4-benzoxazin-3-(4H)-one (1.1 g) is stirred with a half equivalent of sodium borohydride in 30 ml of ethanol/THF 1:1 for three hours at room temperature. The mixture is poured onto water, extracted with ethyl acetate, the organic phase is dried with magnesium sulfate and concentrated by evaporation. A yield of 95% results.

후처리

  1. additionThe mixture is poured onto water
  2. extractionextracted with ethyl acetate
  3. dry with materialthe organic phase is dried with magnesium sulfate
  4. concentrationconcentrated by evaporation
  5. customA yield of 95% results

출처 및 근거

ORD 기록
ord-7c288a0a8602452099e043334a01f3dd
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06365736B1

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