Water → HCID 11601755、化合物

HRID 254244ノート

反応式

HRID 254244 の反応式
[CH:1]12[CH2:13][CH:4]([C:5]3[C:6]([OH:12])=[CH:7][CH:8]=[C:9]([OH:11])[C:10]=31)[CH2:3][CH2:2]2.B(F)(F)F.CCOCC.[Cl:23][CH2:24][CH2:25][C:26]([CH3:30])(O)[CH:27]=[CH2:28].O>O1CCOCC1>[Cl:23][CH2:24][CH2:25][C:26]1([CH3:30])[CH2:27][CH2:28][C:7]2[C:6](=[C:5]3[CH:4]4[CH2:13][CH:1]([CH2:2][CH2:3]4)[C:10]3=[C:9]([OH:11])[CH:8]=2)[O:12]1

参加物

6

反応物 4

HCID 962WaterHCID 8000Boron trifluoride etherateHCID 859671,4-Methanonaphthalene-5,8-diol, 1,2,3,4-tetrahydro-HCID 21494880HCID 21494880、化合物

生成物 1

HCID 11601755HCID 11601755、化合物収率 51.6%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒2 回

反応条件

温度
110 °C

実験手順

A mixture of, 1,2,3,4-tetrahydro-1,4-methano-naphthalene-5,8-diol (1.34 g, 794 mmol), 11.0 ml 3.97 mmol) of BF3.Et2O and 25 ml of dioxane was heated up to 110° C. under a nitrogen atmosphere. A solution of 5-chloro-3-methyl-pent-1-en-3-ol (1.12 g, 8.6 mmol) in 24 ml of dioxane was added slowly to the mixture. The addition was completed after two hours and the mixture was continued to reflux for an additional 3 hours. After cooling down to room temperature, the mixture was poured to water, extracted with ethyl acetate, washed with water and dried over MgSO4. After the removal of solvents, the residue was mixed with methanol/HCl and let stirred overnight at room temperature. After the removal of the solvents the residue was purified via flash column chromatography on silica gel (1:3 EtOAc/Hex) twice to give 1.30 g of 2-(2-chloro-ethyl)-2-methyl-3,4,7,8,9,10-hexahydro-7,10-methano-2H-benzo[h]chromen-6-ol. 1H-NMR (300 MHz, CDCl3) δ (ppm): 6.39 (s, 1H), 4.27 (s, 1H), 3.63-3.47 (m, 4H), 2.73-2.70 (m, 2H), 2.00-1.47 (m, 8H), 1.43-1.15 (m, 4H); MS: 307 (M+H+, 100%).

後処理

  1. additionThe addition
  2. temperatureto reflux for an additional 3 hours
  3. temperatureAfter cooling down to room temperature
  4. extractionextracted with ethyl acetate
  5. washwashed with water
  6. dry with materialdried over MgSO4
  7. customAfter the removal of solvents
  8. additionthe residue was mixed with methanol/HCl
  9. customAfter the removal of the solvents the residue
  10. customwas purified via flash column chromatography on silica gel (1:3 EtOAc/Hex) twice

出典と根拠

ORDレコード
ord-d82e7a61a3f047038a5ac064af30b8d7
出典データセット
uspto-grants-2011_01
特許番号
US07875607B2

反応ノート

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