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Triethylamine → O-(tert-Butyldiphenylsilyl)hydroxylamine

HRID 1788677
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HRID 1788677 반응식
Cl.[NH2:2][OH:3].C(N(CC)CC)C.[Si:11](Cl)([C:24]([CH3:27])([CH3:26])[CH3:25])([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>CN(C=O)C>[Si:11]([O:3][NH2:2])([C:24]([CH3:27])([CH3:26])[CH3:25])([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 94078tert-ButyldiphenylchlorosilaneHCID 443297Hydroxyamine hydrochloride

생성물 1

HCID 11737343O-(tert-Butyldiphenylsilyl)hydroxylamine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Hydroxylamine hydrochloride (3.48 g) and triethylamine (7 ml) were stirred for 0.25 hours in DMF (50 ml) at 0° C. tert-Butyldiphenylsilyl chloride (13 ml) was added and the mixture was stirred for 1 hour. The mixture was partitioned between pentane (500 ml) and water (100 ml), the layers separated and the aqueous phase extracted with ethyl acetate (2×100 ml). The organic layers were combined, washed with brine (50 ml), dried over magnesium sulphate and the solvent was removed in vacuo. The crude product was triturated with pentane (20 ml) yielding the pure title compound as white solid (4.04 g), m.p.t. 85°-87° C.

후처리

  1. additionwas added
  2. customThe mixture was partitioned between pentane (500 ml) and water (100 ml)
  3. customthe layers separated
  4. extractionthe aqueous phase extracted with ethyl acetate (2×100 ml)
  5. washwashed with brine (50 ml)
  6. dry with materialdried over magnesium sulphate
  7. customthe solvent was removed in vacuo
  8. customThe crude product was triturated with pentane (20 ml)

출처 및 근거

ORD 기록
ord-87387689be1e4fb4aa903dde6aeb2236
출처 데이터셋
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04684641

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