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N,N-Diphenylcarbamic chloride → HCID 15550612, 화합물

HRID 1250093
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HRID 1250093 반응식
[CH3:1][O:2][C:3](=[O:15])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([CH2:12][OH:13])[C:7]=1[Cl:14].C[Si]([N-][Si](C)(C)C)(C)C.[K+].[C:26]1([N:32]([C:36]2[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=2)[C:33](Cl)=[O:34])[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>O1CCCC1>[CH3:1][O:2][C:3](=[O:15])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([CH2:12][O:13][C:33](=[O:34])[N:32]([C:36]2[CH:37]=[CH:38][CH:39]=[CH:40][CH:41]=2)[C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:7]=1[Cl:14]
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참가 물질

5

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HCID 65741N,N-Diphenylcarbamic chlorideHCID 3251421Potassium bis(trimethylsilyl)amideHCID 15550611Methyl 2-[2-chloro-3-(hydroxymethyl)phenoxy]acetate

생성물 1

HCID 15550612HCID 15550612, 화합물수율 48%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
-78 °C

실험 절차

A solution of (2-chloro-3-hydroxymethylphenoxy)acetic acid methyl ester (1.94 g, 8.41 mmol) in tetrahydrofuran was cooled to −78° C., treated with potassium bis(trimethylsilyl)amide (10.1 mmol), and allowed to stir at −78° C. for about an hour. A solution of diphenylcarbamyl chloride (2.92 g, 12.6 mmol) in tetrahydrofuran was added dropwise, and the resulting mixture was allowed to warm to room temperature and stirred overnight. The mixture was quenched with water, diluted with diethyl ether, and the layers were separated. The aqueous layer was extracted twice more with diethyl ether. The combined organic extracts were dried over sodium sulfate and concentrated in vacuo. Purification of the residue by silica gel flash chromatography, eluting with hexane/acetone (4:1), gave {2-chloro-3-[(diphenyl-carbamoyloxy)methyl]phenoxy}acetic acid methyl ester as a white crystalline solid (1.72g, 48.0%).

후처리

  1. temperatureto warm to room temperature
  2. stirringstirred overnight
  3. customThe mixture was quenched with water
  4. additiondiluted with diethyl ether
  5. customthe layers were separated
  6. extractionThe aqueous layer was extracted twice more with diethyl ether
  7. dry with materialThe combined organic extracts were dried over sodium sulfate
  8. concentrationconcentrated in vacuo
  9. customPurification of the residue by silica gel flash chromatography
  10. washeluting with hexane/acetone (4:1)

출처 및 근거

ORD 기록
ord-cf543492742e40a59571c1f389a36a4e
출처 데이터셋
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06335459B1

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