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Tin tetrachloride → HCID 15490887, 화합물

HRID 1954257
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HRID 1954257 반응식
[CH:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=1[O:13][CH3:14])[C:7]([OH:9])=O)([CH3:3])[CH3:2].C(Cl)(=O)C(Cl)=O.[Sn](Cl)(Cl)(Cl)Cl.[CH2:26]([C:33]1[S:34][C:35]([CH3:39])=[C:36]([CH3:38])[CH:37]=1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>C(Cl)Cl>[CH2:26]([C:33]1[S:34][C:35]([CH3:39])=[C:36]([CH3:38])[C:37]=1[C:7]([C:6]1[CH:10]=[CH:11][C:12]([O:13][CH3:14])=[C:4]([CH:1]([CH3:2])[CH3:3])[CH:5]=1)=[O:9])[C:27]1[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 24287Tin tetrachlorideHCID 65578Oxalyl chlorideHCID 102419632,3-Dimethyl-5-benzylthiopheneHCID 150525974-Methoxy-3-isopropylbenzoic acid

생성물 1

HCID 15490887HCID 15490887, 화합물수율 83%

시약·촉매·용매 1

HCID 6344Dichloromethane
용매
2회

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온도
-78 °C

실험 절차

At ambient temperature, to a stirred solution containing 3-isopropyl-4-methoxybenzoic acid (27.00 g, 0.139 mol, RN-33537-78-9) and oxalyl chloride (13.3 mL, 0.153 mol) in CH2Cl2 (460 mL) was added N,N-DMF (5 drops). After 2 h, the reaction was cooled to -78° C. To the reaction was added tin (IV) chloride (17.89 mL, 0.153 mol) followed by a solution of 2-benzyl-4,5-dimethylthiophene (28.12 g, 0.139 mol) in CH2Cl2 (120 mL) that had been previously cooled to -78° C. After the addition was complete, the dry ice/acetone bath was removed and the reaction was stirred for 18 h, eventually warming to ambient temperature. The reaction was quenched into H2O (2 L) and extracted with ether. The combined ethereal extracts were sequentially washed with 1N HCl (3×500 mL), H2O (2×500 mL), NaHCO3 (2×500 mL), brine (1×500 mL), dried (MgSO4) and concentrated. Purification on silica gel, eluting with 5% EtOAc/pet. ether, gave 43.65 g (83%) of the title compound as an oil. 1H NMR (DMSO-d6) δ 1.13 (s, 3 H), 1.15 (s, 3 H), 1.81 (s, 3 H), 2.26 (s, 3 H), 3.23 (q, 1 H), 3.85 (s, 2 H), 3.88 (s, 3 H), 7.04-7.24 (m, 6 H), 7.55 (dd, 1 H), 7.63 (d, 1 H).

후처리

  1. temperaturehad been previously cooled to -78° C
  2. additionAfter the addition
  3. customthe dry ice/acetone bath was removed
  4. temperatureeventually warming to ambient temperature
  5. customThe reaction was quenched into H2O (2 L)
  6. extractionextracted with ether
  7. washThe combined ethereal extracts were sequentially washed with 1N HCl (3×500 mL), H2O (2×500 mL), NaHCO3 (2×500 mL), brine (1×500 mL)
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated
  10. customPurification on silica gel
  11. washeluting with 5% EtOAc/pet. ether

출처 및 근거

ORD 기록
ord-8faf2e2c1beb4d3dae055c0c7d3d2f43
출처 데이터셋
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06121271

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