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Chlorotrimethylsilane → N-(Triphenylmethyl)-D-serine

HRID 389378
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HRID 389378 반응식
[NH2:1][C@@H:2]([C:5]([OH:7])=[O:6])[CH2:3][OH:4].C[Si](Cl)(C)C.[C:13](Cl)([C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>ClCCl.CO.C(N(CC)CC)C>[C:13]([NH:1][C@@H:2]([C:5]([OH:7])=[O:6])[CH2:3][OH:4])([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([C:26]1[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=1)[C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 6397ChlorotrimethylsilaneHCID 6456Trityl chlorideHCID 71077D-Serine

생성물 1

HCID 12042811N-(Triphenylmethyl)-D-serine

시약·촉매·용매 3

HCID 887Methanol용매2회HCID 6344Dichloromethane용매3회
HCID 8471
Triethylamine
용매
2회

실험 절차

To dichloromethane (500 ml), D-serine (50 g) was added at ambient temperature under nitrogen atmosphere to form a suspension and then trimethylsilyl chloride (180.91 g) was added to the suspension in 10-15 minutes at ambient temperature. The reaction mixture was refluxed at 35° C. to 40° C. for 20 minutes and then it was cooled to ambient temperature. To the reaction mixture, a solution of triethyl amine (168.50 g) in dichloromethane (50 ml) was added in 30-45 minutes at 25° C. to 30° C. The mixture was refluxed for 45 minutes at 35° C. to 40° C. and then cooled to 0° C. To this mixture, a solution of anhydrous methanol (22.83 g) in dichloromethane (50 ml) was added at 0° C. and the mixture was allowed to reach at room temperature. Triethylamine (48.14 g) was slowly added to it at 25° C. to 30° C. and then trityl chloride (132.63 g) was added in 3 lots to the mixture at an interval of 10 minutes. The reaction mixture was then stirred for 3 hours under nitrogen at ambient temperature. After completion of the reaction, methanol (76.12 g) was added at ambient temperature in 10-15 minutes and the solvent was recovered under vacuum at 40° C. to 45° C. The crude product obtained was washed with water (750 ml) and filtered. The filtered product was further washed with 5% citric acid solution (750 ml) and filtered. The solid product obtained was partitioned between water (750 ml) and hexanes (200 ml) and then filtered. The filtered solid was washed with hexanes (200 ml) and dried to obtain the titled product. Yield=135 gm.

후처리

  1. customto form a suspension
  2. temperatureThe reaction mixture was refluxed at 35° C. to 40° C. for 20 minutes
  3. temperatureThe mixture was refluxed for 45 minutes at 35° C. to 40° C.
  4. temperaturecooled to 0° C
  5. customto reach at room temperature
  6. additionwas added at ambient temperature in 10-15 minutes
  7. customthe solvent was recovered under vacuum at 40° C. to 45° C
  8. customThe crude product obtained
  9. washwas washed with water (750 ml)
  10. filtrationfiltered
  11. washThe filtered product was further washed with 5% citric acid solution (750 ml)
  12. filtrationfiltered
  13. customThe solid product obtained
  14. customwas partitioned between water (750 ml) and hexanes (200 ml)
  15. filtrationfiltered
  16. washThe filtered solid was washed with hexanes (200 ml)
  17. customdried

출처 및 근거

ORD 기록
ord-4eb15919b2ae4277a6e0db6813ef692b
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08378142B2

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