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Carbon tetrabromide → HCID 53304915、化合物

HRID 2168580
ノート
印刷プレビュー

反応式

HRID 2168580 の反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Cl:20][C:21]1[CH:48]=[CH:47][C:24]([C:25]([O:27][CH2:28][C@@H:29]2[C@@H:33]([O:34][C:35](=[O:43])[C:36]3[CH:41]=[CH:40][C:39]([Cl:42])=[CH:38][CH:37]=3)[C@:32]([F:45])([CH3:44])[C@H:31](O)[O:30]2)=[O:26])=[CH:23][CH:22]=1.C(Br)(Br)(Br)[Br:50].C1(P(=O)(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>ClCCl>[Cl:42][C:39]1[CH:40]=[CH:41][C:36]([C:35]([O:34][C@H:33]2[C@:32]([F:45])([CH3:44])[C@@H:31]([Br:50])[O:30][C@@H:29]2[CH2:28][O:27][C:25](=[O:26])[C:24]2[CH:47]=[CH:48][C:21]([Cl:20])=[CH:22][CH:23]=2)=[O:43])=[CH:37][CH:38]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 11205Carbon tetrabromideHCID 11776TriphenylphosphineHCID 13097Triphenylphosphine OxideHCID 53304768(2R,3R,4R,5R)-2-[(4-chlorobenzoyloxy)methyl]-4-fluoro-5-hydroxy-4-methyloxolan-3-yl 4-chlorobenzoate

生成物 1

HCID 53304915HCID 53304915、化合物

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

反応条件

温度
-22 °C

実験手順

Anhydrous dichloromethane (530 mL) was added to a 1 L of dry round-bottomed flask and cooled to −22° C. Triphenylphosphine (19.5 g, 74 mmol) was added and then added the β-lactol (2b, 23.5 g, 53 mmol). To that solution, carbon tetrabromide (26.3 g, 79.5 mmol, solid) was added portionwise over 5 min. at −22° C. The reaction was slowly warmed up to room temperature and once reaction was complete, the solution was passed through a short pad of silica gel (148 g in a 600 mL of fritted disc Buchner funnel) to remove any brown color polar impurities. The colorless filtrate was concentrated to dryness under reduced pressure and the solid residue was dissolved in ethyl ether (170 mL). Hexanes (50 mL) was added slowly until a precipitate started to form. The product was collected as a light yellow solid via filtration and dried (0.2 mm Hg, 25° C., 17 h) to afford 21.23 g, (79%) with an anomeric ratio of α/β>65:1. The product was contaminated with 3-4% of triphenylphosphine oxide which had no effect on the next reaction step. 1H NMR (CDCl3): δ 8.05 (m, 2H, arom.), 7.95 (m, 2H, arom.), 7.47-7.40 (m, 4H, arom.), 6.33 (s, 1H, C1-H), 5.22 (m, 1H, C3-H), 4.84 (m, 1H, C4-H), 4.76 (m, 1H, C5-Ha), 4.62 (m, 1H, C5-Hb), 1.69 (d, 3H, CH3, J=21.6 Hz).

後処理

  1. temperatureThe reaction was slowly warmed up to room temperature
  2. customonce reaction
  3. customto remove any brown color polar impurities
  4. concentrationThe colorless filtrate was concentrated to dryness under reduced pressure
  5. dissolutionthe solid residue was dissolved in ethyl ether (170 mL)
  6. additionHexanes (50 mL) was added slowly until a precipitate
  7. customto form
  8. filtrationThe product was collected as a light yellow solid via filtration
  9. customdried (0.2 mm Hg, 25° C., 17 h)
  10. customto afford 21.23 g, (79%) with an anomeric ratio of α/β>65:1
  11. customon the next reaction step

出典と根拠

ORDレコード
ord-af0df77f603548049e3e4001524daf57
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09045520B2

反応ノート

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