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Bromothymol Blue → Tetraethyl 3-benzylaminopentane-1,1-bisphosphonate

HRID 1971
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HRID 1971 반응식
O=[C:2]([CH2:21][CH3:22])[CH2:3][CH:4]([P:13]([O:18][CH2:19][CH3:20])(=[O:17])[O:14][CH2:15][CH3:16])[P:5]([O:10][CH2:11][CH3:12])(=[O:9])[O:6][CH2:7][CH3:8].CC1C(C2(C3C(C)=C(Br)C(O)=C(C(C)C)C=3)OS(=O)(=O)C3C2=CC=CC=3)=CC(C(C)C)=C(O)C=1Br.[CH2:58]([NH2:65])[C:59]1[CH:64]=[CH:63][CH:62]=[CH:61][CH:60]=1.[BH3-]C#N.[Na+]>CO.C(O)(=O)C>[CH2:58]([NH:65][CH:2]([CH2:21][CH3:22])[CH2:3][CH:4]([P:13]([O:18][CH2:19][CH3:20])(=[O:17])[O:14][CH2:15][CH3:16])[P:5]([O:10][CH2:11][CH3:12])(=[O:9])[O:6][CH2:7][CH3:8])[C:59]1[CH:64]=[CH:63][CH:62]=[CH:61][CH:60]=1
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참가 물질

7

반응물 4

HCID 6450Bromothymol BlueHCID 7504BenzylamineHCID 5003444Sodium cyanoborohydride2회HCID 12499407Tetraethyl 3-oxopentane-1,1-bisphosphonate

생성물 1

HCID 19689047Tetraethyl 3-benzylaminopentane-1,1-bisphosphonate

시약·촉매·용매 2

HCID 176
Acetic Acid
용매
HCID 887Methanol용매

실험 절차

To a stirred solution of tetraethyl 3-oxopentane-1,1-bisphosphonate (0.50 g, 1.4 mmol) in methanol (5 ml) was added a small amount of bromothymol blue and benzylamine (0.75 g, 7.0 mmol). Acetic acid was added dropwise until the solution turned yellow (pH=6), and NaCNBH3 (57 mg, 0.9 mmol) was added. The resulting yellow solution was stirred at room temperature for 2 days, at which time more NaCNBH3 (20 mg) was added. After stirring a total of 4 days, the reaction was quenched by adding concentrated HCl until the pH was less than 1, and the solvents were removed in vacuo. The residue was taken up in water (10 ml) and washed with diethyl ether (2×20 ml). The aqueous layer was made basic (pH greater than 10) by the addition of solid KOH, saturated with NaCl, and extracted with dichloromethane (5×25 ml). The combined extracts were dried (Na2SO4) and concentrated to give tetraethyl 3-benzylaminopentane-1,1-bisphosphonate. This material was hydrolyzed by heating at reflux in concentrated HCl (6 ml) for 20 hours. The volatiles were removed under vacuum, the residue dissolved in water (10 ml) and concentrated under vacuum to give 0.49 g of Compound No. 159 as a hygroscopic foam.

후처리

  1. additionwas added
  2. additionwas added
  3. customthe reaction was quenched
  4. additionby adding concentrated HCl until the pH was less than 1
  5. customthe solvents were removed in vacuo
  6. washwashed with diethyl ether (2×20 ml)
  7. additionby the addition of solid KOH
  8. extractionsaturated with NaCl, and extracted with dichloromethane (5×25 ml)
  9. dry with materialThe combined extracts were dried (Na2SO4)
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-ea7684e9a71040288dbea5e299a3c7d7
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05728650

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