Triethylamine → N-t-butoxycarbonyl-p-hydroxymethylphenylglycine

HRID 1287980

반응식

HRID 1287980 반응식
[OH:1][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][CH2:10][C:11]([OH:13])=[O:12])=[CH:5][CH:4]=1.C(N(CC)CC)C.[C:21]([O:25][C:26](N=[N+]=[N-])=[O:27])([CH3:24])([CH3:23])[CH3:22]>O.O1CCCC1>[C:21]([O:25][C:26]([N:9]([C:6]1[CH:5]=[CH:4][C:3]([CH2:2][OH:1])=[CH:8][CH:7]=1)[CH2:10][C:11]([OH:13])=[O:12])=[O:27])([CH3:24])([CH3:23])[CH3:22]

참가 물질

6

실험 절차

To a solution of p-hydroxymethylphenylglycine (8.0 g, 0.044 mole) and triethylamine (8.8 g., 0.087 mole) in 160 ml water was added t-butoxycarbonyl azide (6.95 g., 0.049 mole) dissolved in 120 ml tetrahydrofuran. After stirring overnight at room temperature, the reaction mixture was washed twice with 200 ml. portions of ether. The aqueous layer was covered with ether and in an ice bath was acidified to pH 3-3.5 with 3N hydrochloric acid. The acidic solution was extracted three times with 200 ml portions of ether. The combined ether layers were washed with saturated sodium chloride solution, dried, and the ether evaporated under reduced pressure. The resulting oil was triturated with chloroform-hexane and the solid filtered off to give N-t-butoxycarbonyl-p-hydroxymethylphenylglycine (7.74 g, 63% yield), m.p. 139°-141.5° (dec.).

후처리

  1. washthe reaction mixture was washed twice with 200 ml
  2. customThe aqueous layer was covered with ether and in an ice bath
  3. extractionThe acidic solution was extracted three times with 200 ml portions of ether
  4. washThe combined ether layers were washed with saturated sodium chloride solution
  5. customdried
  6. customthe ether evaporated under reduced pressure
  7. customThe resulting oil was triturated with chloroform-hexane
  8. filtrationthe solid filtered off

출처 및 근거

ORD 기록
ord-d17c99bf46754632a68507d7b50f8d04
출처 데이터셋
uspto-grants-1976_10
특허 번호
US03987041

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