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Tetrahydrofuran → HCID 22805384, 화합물

HRID 1449250
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HRID 1449250 반응식
[CH3:1][C@@:2]1([C:8](O)=[O:9])[CH2:6][CH2:5][C:4](=[O:7])[O:3]1.O1CCCC1>O>[OH:9][CH2:8][C@@:2]1([CH3:1])[O:3][C:4](=[O:7])[CH2:5][CH2:6]1
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참가 물질

4

반응물 2

HCID 8028TetrahydrofuranHCID 53249432(2S)-2-Methyl-5-oxooxolane-2-carboxylic acid

생성물 1

HCID 22805384HCID 22805384, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a solution of 14.8 g. (102.7 mmol) of (S)-(-)-2-methyl-5-oxotetrahydro-2-furoic acid mp 84°-87° C.; [α]25D-16.56° in 70 ml. of dry tetrahydrofuran (THF) was added 10.1 ml. (8.1 g.; 106.7 mmol) of borane-methyl sulphide complex, dropwise, with stirring over a 0.5 hr. period. Occasional ice-bath cooling was employed to maintain the internal temperature below 30°. After stirring at room temperature for 1.5 hr., the reaction mixture was cautiously decomposed by the dropwise addition of 6.2 ml. of H2O. The mixture was then concentrated under water aspirator pressure and the residue was taken up in ethyl acetate and filtered. The solids were washed thoroughly with ethyl acetate and filtered. The solids were washed thoroughly with ethyl acetate and the filtrate and washes were combined and concentrated in vacuo giving (S)-(+)-5-(hydroxymethyl)-5-methyldihydro-2(3H)-furanone as a colorless oil (13.6 g.) which was used without further purification.

후처리

  1. temperatureOccasional ice-bath cooling
  2. temperatureto maintain the internal temperature below 30°
  3. stirringAfter stirring at room temperature for 1.5 hr
  4. addition, the reaction mixture was cautiously decomposed by the dropwise addition of 6.2 ml
  5. concentrationThe mixture was then concentrated under water aspirator pressure
  6. filtrationfiltered
  7. washThe solids were washed thoroughly with ethyl acetate
  8. filtrationfiltered
  9. washThe solids were washed thoroughly with ethyl acetate
  10. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-07c347a2e6b24315930c21e9fc797c3d
출처 데이터셋
uspto-grants-1980_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04189612

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