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Taurine → HCID 57345279, 화합물

HRID 1794970
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HRID 1794970 반응식
[NH2:1][CH2:2][CH2:3][S:4]([OH:7])(=[O:6])=[O:5].[CH2:8]([O:15][C:16](Cl)=[O:17])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.C(=O)(O)[O-].[Na+:23]>[OH-].[Na+].O>[Na+:23].[CH2:8]([O:15][C:16]([NH:1][CH2:2][CH2:3][S:4]([O-:7])(=[O:6])=[O:5])=[O:17])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 1123TaurineHCID 10387Benzyl chloroformateHCID 516892Sodium Bicarbonate

생성물 1

HCID 57345279HCID 57345279, 화합물수율 14%

시약·촉매·용매 2

HCID 962Water용매HCID 14798Sodium Hydroxide용매2회

실험 절차

Taurine, 1 (about 40 g, 320 mmols), was dissolved in 4N sodium hydroxide solution (80 mL) and water (about 200 mL). To this solution was added benzyloxycarbonyl chloride, (about 48 mL, 330 mmols) dropwise, with vigorous stirring during a period of about 4 hours. The pH of the solution was maintained alkaline by the addition of 10% sodium bicarbonate solution (about 300 mL) and 4N sodium hydroxide solution (about 45 mL). The obtained reaction mixture was then washed with diethyl ether (about 1000 mL) and the aqueous layer was rotary evaporated to dryness, and further dried under high vacuum over phosphorous pentoxide overnight to yield about 12.7 g (14%) of 2. 1H-NMR (D2O): δ 7.50 (5H, s, Ar—H), 5.21 (2H, s, Ar—CH2), 3.62 (2H, t, CH2), 3.14 (2H, t, CH2).

후처리

  1. temperatureThe pH of the solution was maintained alkaline
  2. customThe obtained reaction mixture
  3. washwas then washed with diethyl ether (about 1000 mL)
  4. customthe aqueous layer was rotary evaporated to dryness
  5. dry with materialfurther dried under high vacuum over phosphorous pentoxide overnight

출처 및 근거

ORD 기록
ord-cc4e1ce43f2f4d1091ebee4380714992
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07025987B2

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