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Benzyl Alcohol → 3,5-Bis(decyloxy)phenylcarbamic acid phenylmethyl ester

HRID 1110213
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HRID 1110213 반응식
[CH2:1]([O:11][C:12]1[CH:13]=[C:14]([CH:18]=[C:19]([O:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[CH:20]=1)C(O)=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:39])C=CC=CC=1.C([N:51]([CH2:54]C)CC)C.[CH2:56]([OH:63])[C:57]1[CH:62]=[CH:61][CH:60]=[CH:59][CH:58]=1>C1(C)C=CC=CC=1>[C:57]1([CH2:56][O:63][C:54](=[O:39])[NH:51][C:14]2[CH:18]=[C:19]([O:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[CH:20]=[C:12]([O:11][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])[CH:13]=2)[CH:62]=[CH:61][CH:60]=[CH:59][CH:58]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 244Benzyl AlcoholHCID 8471TriethylamineHCID 199401P,P-Diphenylphosphinic azideHCID 10320747Benzoic acid, 3,5-bis(decyloxy)-

생성물 1

HCID 99847623,5-Bis(decyloxy)phenylcarbamic acid phenylmethyl ester수율 79%

시약·촉매·용매 1

HCID 1140
Toluene
용매

실험 절차

To a stirred, ice bath cooled solution of 5.0 g (0.0115 mol) of 3,5-bis(decyloxy)benzoic acid in 100 ml of anhydrous toluene was added dropwise 3.0 ml (0.0138 mol) of diphenylphosphoryl azide followed by dropwise solution of 1.9 ml (0.0138 mol) of triethylamine. The reaction mixture was stirred in the ice bath for 75 minutes and then was heated at 90° for 2 hours. Benzyl alcohol (100 ml) was added and the solution was stirred and heated at 90° for 3.5 hours. The solvent was removed under reduced pressure and most of the excess benzyl alcohol was removed at 80°/0.1 mm. Sodium bicarbonate solution (100 ml) was added to the residue and the product was extracted with ethyl acetate. The dried extract was concentrated at reduced pressure to an oil which was purified by HPLC using 25% hexane-ethyl acetate to give 4.87 g (79% yield) of 3,5-bis(decyloxy)phenylcarbamic acid phenylmethyl ester as an oil.

후처리

  1. temperaturewas heated at 90° for 2 hours
  2. temperatureheated at 90° for 3.5 hours
  3. customThe solvent was removed under reduced pressure and most of the excess benzyl alcohol
  4. customwas removed at 80°/0.1 mm
  5. additionSodium bicarbonate solution (100 ml) was added to the residue
  6. extractionthe product was extracted with ethyl acetate
  7. extractionThe dried extract
  8. concentrationwas concentrated at reduced pressure to an oil which
  9. customwas purified by HPLC

출처 및 근거

ORD 기록
ord-a8bf2df8cf444b3fbf6969c7b975e0fd
출처 데이터셋
uspto-grants-1994_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05324747

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