2,3-Naphthalenedicarboxylic acid → 2,3-Bis(hydroxymethyl)naphthalene

HRID 487887

반응식

HRID 487887 반응식
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[C:3]([C:11](O)=[O:12])[C:2]=1[C:14](O)=[O:15].[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[OH:12][CH2:11][C:3]1[C:2]([CH2:14][OH:15])=[CH:1][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=1

참가 물질

4

실험 절차

A solution of 2,3-naphthalenedicarboxylic acid (4.6 g, 0.023 mole) in dry THF (135 mL, wanned to 50° C. to maintain solution) is added dropwise over 15 minutes to a 1.15 M lithium aluminum hydride solution in THF (45 mL, 0.052 mole). The solution is stirred 3 hours after which TLC indicated consumption of diacid and formation of a new major product. The reaction is quenched carefully with THF-water, then 2N hydrochloric acid (40 mL) is added, and the resulting mixture is extracted 3 times with ether. The combined ether extracts are washed with water (2 times), with saturated sodium bicarbonate solution (1 time), with water, and are dried (sodium sulfate), filtered, and concentrated to give a tan solid (3.67 g). The solid is recrystallized from ethyl acetate giving the title compound (2.91 g) as a light tan crystalline material, mp 161°-162° C. (lit. ref mp 160° C.).

후처리

  1. customconsumption of diacid and formation of a new major product
  2. customThe reaction is quenched carefully with THF-water
  3. addition2N hydrochloric acid (40 mL) is added
  4. extractionthe resulting mixture is extracted 3 times with ether
  5. washThe combined ether extracts are washed with water (2 times), with saturated sodium bicarbonate solution (1 time), with water
  6. dry with materialare dried (sodium sulfate)
  7. filtrationfiltered
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f9c5095c8d144c6aa478d87d79b9ddf2
출처 데이터셋
uspto-grants-1994_03
특허 번호
US05298498

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