ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Triphenylphosphine → (R)-6-Bromo-11-[3,5-dibromo-4-(1-bromomethyl-2-phenyl-ethoxy)-phenyl]-benzo[b]naphtho[2,3-d]thiophene

HRID 1873201
ノート
印刷プレビュー

反応式

HRID 1873201 の反応式
CCOC(/N=N/C(OCC)=O)=O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Br-:32].[Li+].[Br:34][C:35]1[C:47]2[S:46][C:45]3[CH:48]=[CH:49][CH:50]=[CH:51][C:44]=3[C:43]=2[C:42]([C:52]2[CH:57]=[C:56]([Br:58])[C:55]([O:59][C@@H:60]([CH2:68]O)[CH2:61][C:62]3[CH:67]=[CH:66][CH:65]=[CH:64][CH:63]=3)=[C:54]([Br:70])[CH:53]=2)=[C:41]2[C:36]=1[CH:37]=[CH:38][CH:39]=[CH:40]2>C1COCC1>[Br:34][C:35]1[C:47]2[S:46][C:45]3[CH:48]=[CH:49][CH:50]=[CH:51][C:44]=3[C:43]=2[C:42]([C:52]2[CH:53]=[C:54]([Br:70])[C:55]([O:59][C@@H:60]([CH2:68][Br:32])[CH2:61][C:62]3[CH:63]=[CH:64][CH:65]=[CH:66][CH:67]=3)=[C:56]([Br:58])[CH:57]=2)=[C:41]2[C:36]=1[CH:37]=[CH:38][CH:39]=[CH:40]2
参加物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 11776TriphenylphosphineHCID 82050Lithium BromideHCID 5462977Diethyl azodicarboxylateHCID 53810433(R)-6-Bromo-11-[3,5-dibromo-4-(1-hydroxymethyl-2-phenyl-ethoxy)-phenyl]-benzo[b]naphtho[2,3-d]thiophene

生成物 1

HCID 53895472(R)-6-Bromo-11-[3,5-dibromo-4-(1-bromomethyl-2-phenyl-ethoxy)-phenyl]-benzo[b]naphtho[2,3-d]thiophene収率 73%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

Diethylazodicarboxylate (0.151 mL, 0.96 mmol) was added dropwise to a 0° C., stirred solution of triphenylphosphine (0.257 g, 0.98 mmol) in THF (6 mL) under a dry nitrogen atmosphere. After 20 min., lithium bromide was added to a nearly colorless reation mixture, followed by adding a solution of (R)-6-bromo-1 1-[3,5-dibromo-4-(1-hydroxymethyl-2-phenyl-ethoxy)-phenyl]-benzo[b]naphtho[2,3-d]thiophene (0.273 g, 0.392 mmol) in THF (3 mL). After 1 h, the solution was allowed to warm to ambient temperature. After 2 h, the reaction mixture was quenched with water (0.2 mL) and further diluted with ethyl ether (50 mL). Silica gel (8 mL) was added. Solvent was removed and the silica adsorbate was flash chromatographed (eluent 98:2 petroleum ether:ethyl acetate) to provide the title compound as a white solid (0.23 g, 73%): mp >90° C. (dec.): MS (EI): [M+], 4 bromine isotope pattern, 756, 758, 760, 762, 764; Anal. Calc. for C28H17Br3N203S.0.25 hexane: C, 49.97, H, 2.97, N, 0.00. Found: C, 49.97, H, 2.83, N, 0.02.

後処理

  1. waitAfter 1 h
  2. waitAfter 2 h
  3. customthe reaction mixture was quenched with water (0.2 mL)
  4. additionfurther diluted with ethyl ether (50 mL)
  5. additionSilica gel (8 mL) was added
  6. customSolvent was removed
  7. customchromatographed (eluent 98:2 petroleum ether:ethyl acetate)

出典と根拠

ORDレコード
ord-2f26905b81ae4259bcceb9df97c8c2bf
出典データセット
uspto-grants-2000_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06110962

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート