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Triethylamine → HCID 131723537、化合物

HRID 990615
ノート
印刷プレビュー

反応式

HRID 990615 の反応式
C(N(CC)CC)C.[O:8]([C:16]1[CH:17]=[C:18]([CH:23]=[CH:24][CH:25]=1)[C:19]([O:21][CH3:22])=O)[Si:9]([C:12]([CH3:15])([CH3:14])[CH3:13])([CH3:11])[CH3:10].[C:26]1([C:32]2[CH:33]3[C:46](=O)[CH:37]([CH:38]([C:40]4[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=4)[CH:39]=2)[CH2:36][CH2:35][CH2:34]3)[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>C1COCC1.CCCCCC.[Zn]>[O:8]([C:16]1[CH:17]=[C:18]([CH2:19][O:21][CH:22]=[C:36]2[CH2:35][CH2:34][CH:33]3[CH2:46][CH:37]2[CH:38]([C:40]2[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=2)[CH:39]=[C:32]3[C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:23]=[CH:24][CH:25]=1)[Si:9]([C:12]([CH3:15])([CH3:14])[CH3:13])([CH3:11])[CH3:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 8471TriethylamineHCID 2728532,4-Diphenylbicyclo[3.3.1]non-2-en-9-one2 回HCID 11715937Benzoic acid, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, methyl ester

生成物 1

HCID 131723537HCID 131723537、化合物

試薬・触媒・溶媒 3

HCID 23994Zinc触媒HCID 8028
Tetrahydrofuran
溶媒
3 回
HCID 8058Hexane溶媒

実験手順

Into a 1000 mL three-neck flask equipped with magnetic stirrer, pressure-equalizing addition funnel and nitrogen line was charged with 200 mL of anhydrous THF. Ttitanium tetrachloride (17 mL) was added dropwise over a period of 30 minutes. The suspension was stirred for 20 minutes and 25.5 parts of zinc was added in small portions . The reaction mixture was heated under reflux for 2 hours and 42.5 mL of triethylamine was added dropwise. After refluxing one hour, 9 parts of a solution of methyl 3-tert-butyldimethylsiloxybenzoate and 4 parts of ketone (77) in 100 mL of dry THF was added over a period of 60 minutes and the reaction mixture was heated for one hour. The mixture on TLC silica gel plate showed the presence of the starting ester. An additional 1 part of starting ketone (77) in 35 mL of dry THF was added dropwise over 45 minutes and refluxed for two hours. The mixture was cooled to room temperature, diluted with 600 mL of hexane and decanted. The residue was washed with 3×250 mL of hexane. The combined hexane layer was filtered and evaporated under reduced pressure to give an oily material which was purified by chromatography on silica gel column using 5% ethyl acetate/hexane as an eluant. The fractions were checked by TLC on silica gel plate and the desired fractions were combined. The solvent was evaporated under reduced pressure to give an oil, yield 9.6 parts.

後処理

  1. customInto a 1000 mL three-neck flask equipped with magnetic stirrer, pressure-equalizing addition funnel
  2. temperatureThe reaction mixture was heated
  3. temperatureunder reflux for 2 hours
  4. temperatureAfter refluxing one hour
  5. temperaturethe reaction mixture was heated for one hour
  6. temperaturerefluxed for two hours
  7. customdecanted
  8. washThe residue was washed with 3×250 mL of hexane
  9. filtrationThe combined hexane layer was filtered
  10. customevaporated under reduced pressure
  11. customto give an oily material which
  12. customwas purified by chromatography on silica gel column
  13. customThe solvent was evaporated under reduced pressure
  14. customto give an oil
  15. customyield 9.6 parts

出典と根拠

ORDレコード
ord-ee8e11ddf7d146269a4cdb4cd06c732f
出典データセット
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06461876B1

反応ノート

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