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Sodium Bicarbonate → HCID 136196396, 화합물

HRID 1731983
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HRID 1731983 반응식
[C:1]([C:6]1[C:7](=[O:19])[CH2:8][CH:9]([CH:13]2[CH2:18][CH2:17][CH2:16][S:15][CH2:14]2)[CH2:10][C:11]=1[OH:12])(=O)[CH2:2][CH2:3][CH3:4].Cl.[O:21]1[CH2:25][CH2:24][CH2:23][CH:22]1[CH2:26][O:27][NH2:28].C(=O)(O)[O-].[Na+]>CO>[OH:12][C:11]1[CH2:10][CH:9]([CH:13]2[CH2:18][CH2:17][CH2:16][S:15][CH2:14]2)[CH2:8][C:7](=[O:19])[C:6]=1[C:1](=[N:28][O:27][CH2:26][CH:22]1[CH2:23][CH2:24][CH2:25][O:21]1)[CH2:2][CH2:3][CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 516892Sodium BicarbonateHCID 22924062HCID 22924062, 화합물HCID 178450332HCID 178450332, 화합물

생성물 1

HCID 136196396HCID 136196396, 화합물수율 81%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

2.82 g (10 millimoles) of 2-butyryl-3-hydroxy-5-(tetrahydrothiopyran-3-yl)-cyclohex-2-en-1-one was stirred together with 1.69 g (11 millimoles) of tetrahydrofur-2-ylmethoxyamine hydrochloride and 0.93 g (11 millimoles) of sodium bicarbonate in 20 ml of methanol for 12 hours at 25° C. The mixture was evaporated down, the residue was taken up with dichlorbmethane and the solution was extracted by shaking with water. The dried dichloromethane solution was evaporated down to give 3.1 g (8.1 millimoles) of 3-hydroxy-2-(1-tetrahydrofur-2-ylmethoxyiminobutyl)-5-(tetrahydrothiopyran-3-yl)-cyclohex-2-en-1-one as a viscous oil. ##STR9##

후처리

  1. customThe mixture was evaporated down
  2. extractionthe solution was extracted
  3. customThe dried dichloromethane solution was evaporated down

출처 및 근거

ORD 기록
ord-528d4030bb9f4755b0af81919798dff7
출처 데이터셋
uspto-grants-1986_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04624696

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