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Hydrochloric Acid → N-[3-(acetylmethylamino)-2-hydroxypropyl]-N-methylacetamide

HRID 76240
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인쇄 미리보기

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HRID 76240 반응식
[C:1]([CH2:4][NH:5][CH2:6][CH:7]([O:14][Si](C(C)(C)C)(C)C)[CH2:8][N:9]([CH3:13])[C:10](=[O:12])[CH3:11])(=[O:3])[CH3:2].Cl>CO>[C:1]([CH2:4][NH:5][CH2:6][CH:7]([OH:14])[CH2:8][N:9]([CH3:13])[C:10](=[O:12])[CH3:11])(=[O:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 86698891N-[3-(acetylmethylamino)-2-(tert-butyldimethyl silanyloxy)propyl]-N-methylacetamide

생성물 1

HCID 86698890N-[3-(acetylmethylamino)-2-hydroxypropyl]-N-methylacetamide수율 95.1%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of N-[3-(acetylmethylamino)-2-(tert-butyldimethyl silanyloxy)propyl]-N-methylacetamide (1.12 g, 3.54 mmol) in methanol (23 mL), hydrogen chloride 4M dioxane solution (0.357 mL, 1.426 mmol) was added dropwise at 0° C. and the reaction was stirred at r.t. overnight. Solvent was evaporated and the residue triturated with petroleum ether and decanted. The oil obtained after trituration was dried under vacuum affording N-[3-(acetylmethylamino)-2-hydroxypropyl]-N-methylacetamide (681 mg, 95% yield).

후처리

  1. customSolvent was evaporated
  2. customthe residue triturated with petroleum ether
  3. customdecanted
  4. customThe oil obtained after trituration
  5. customwas dried under vacuum

출처 및 근거

ORD 기록
ord-1eca467bf16343c4bf56a6b7ef36026a
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08835494B2

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