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Carbon Dioxide → 5-Methoxy-1-phenyl-1-(pyrrolidin-3-yl)pentan-1-ol

HRID 253553
ノート
印刷プレビュー

反応式

HRID 253553 の反応式
[OH:1][C:2]([CH:15]1[CH2:19][CH2:18][N:17](C(OC(C)(C)C)=O)[CH2:16]1)([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH2:3][CH2:4][CH2:5][CH2:6][O:7][CH3:8].Cl.C([O-])([O-])=O.[K+].[K+].C(=O)=O>CC#N>[CH3:8][O:7][CH2:6][CH2:5][CH2:4][CH2:3][C:2]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)([CH:15]1[CH2:19][CH2:18][NH:17][CH2:16]1)[OH:1]
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 280Carbon DioxideHCID 313Hydrochloric AcidHCID 11430Potassium CarbonateHCID 57786486Tert-butyl 3-(1-hydroxy-5-methoxy-1-phenylpentyl)pyrrolidine-1-carboxylate

生成物 1

HCID 574196125-Methoxy-1-phenyl-1-(pyrrolidin-3-yl)pentan-1-ol収率 66.4%

試薬・触媒・溶媒 1

HCID 6342
Acetonitrile
溶媒

実験手順

To a stirred solution of tert-butyl 3-(1-hydroxy-5-methoxy-1-phenylpentyl)pyrrolidine-1-carboxylate (290 mg, 0.80 mmol) in MeCN (20 mL) was added 5% aq HCl (20 mL). The mixture was stirred at rt for 17 h and solid K2CO3 was added until CO2 evolution ceased. MeCN was removed under reduced pressure and the aqueous residue was extracted with CH2Cl2 (2×90 mL). The combined organic extracts were dried over Na2SO4 and concentrated to afford 5-methoxy-1-phenyl-1-(pyrrolidin-3-yl)pentan-1-ol (140 mg, 66%) as an oil.

後処理

  1. customMeCN was removed under reduced pressure
  2. extractionthe aqueous residue was extracted with CH2Cl2 (2×90 mL)
  3. dry with materialThe combined organic extracts were dried over Na2SO4
  4. concentrationconcentrated

出典と根拠

ORDレコード
ord-c2be04b13f34448bb8fa48466ed67ce2
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07872028B2

反応ノート

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