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Methanol → HCID 88089139, 화합물

HRID 2380189
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HRID 2380189 반응식
[CH2:1]([SH:3])[CH3:2].C[OH:5].CC1C=CC(S([O:16][CH2:17][C@H:18]2[O:22][C@@H:21](OC)[C@@H:20]3OC(C)(C)O[C@H:19]23)(=O)=O)=CC=1>C[O-].[Na+]>[CH2:20]([CH2:19][C@@H:18]([OH:22])[C@@H:17]([OH:16])[C@@H:2]([OH:5])[CH:1]=[S:3])[CH3:21]
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참가 물질

5

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HCID 887MethanolHCID 6343EthanethiolHCID 11013769beta-D-Ribofuranoside, methyl 2,3-O-(1-methylethylidene)-, 5-(4-methylbenzenesulfonate)

생성물 1

HCID 88089139HCID 88089139, 화합물수율 120.2%

시약·촉매·용매 1

HCID 10942334Sodium Methoxide용매

실험 절차

A solution of ethanethiol (11.5 ml, 155 mmol) in 1N sodium methoxide in methanol (150 ml, 150 mmol sodium methoxide) was added to a solution of methyl 2,3-O-isopropylidene-5-O-p-toluenesulfonyl-β-D-ribofuranoside (50 g, 140 mmol in 200 ml dry methanol) and heated at reflux for 24 h. Solvents were removed by evaporation in vacuo, and the sticky residue was taken up in diethyl ether (300 ml) and washed with water (4×100 ml). The ether phase was dried and concentrated in vacuo to furnish a viscous oil. Fractional distillation (70° C. at 0.06 Torr) using a short-path distillation apparatus afforded 30.0 g (86.5% yield) of methyl 5-deoxy-5-ethylthio2,3-O-isopropylidene-β-D-ribofuranoside (III) as a colorless, viscous oil. TLC (silica; 25% ethylacetate in hexane): Rf 0.44 (III); visualization spray as in A above.

후처리

  1. temperatureheated
  2. temperatureat reflux for 24 h
  3. customSolvents were removed by evaporation in vacuo
  4. washwashed with water (4×100 ml)
  5. dry with materialThe ether phase was dried
  6. concentrationconcentrated in vacuo
  7. customto furnish a viscous oil
  8. distillationFractional distillation (70° C. at 0.06 Torr)

출처 및 근거

ORD 기록
ord-29e1fcd2151145ff82e007c3d9dcbf7c
출처 데이터셋
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05366954

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