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5-Azido-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid methyl ester → (5-Amino-5,6,7,8-tetrahydronaphthalen-2-yl)methanol

HRID 32112
ノート
印刷プレビュー

反応式

HRID 32112 の反応式
C[O:2][C:3]([C:5]1[CH:14]=[CH:13][C:12]2[CH:11]([N:15]=[N+]=[N-])[CH2:10][CH2:9][CH2:8][C:7]=2[CH:6]=1)=O>C1COCC1>[NH2:15][CH:11]1[CH2:10][CH2:9][CH2:8][C:7]2[CH:6]=[C:5]([CH2:3][OH:2])[CH:14]=[CH:13][C:12]1=2
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 208244765-Azido-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid methyl ester

生成物 1

HCID 18448553(5-Amino-5,6,7,8-tetrahydronaphthalen-2-yl)methanol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of 5-azido-5,6,7,8-tetrahydro-naphthalene-2-carboxylic acid methyl ester (35 g, 151 mmol, 1.0 eq) in THF (100 mL) was added dropwise in 30 min. The reaction was warmed to RT spontaneously and stirred at RT overnight. The reaction was quenched with THF and H2O mixture (30 mL, THF:H2O=2:1), followed by the sequential addition of 5 N NaOH (10 mL) and H2O (100 mL) while keeping the temperature of the reaction lower than 5° C. The reaction was stirred at RT for additional 5 h. The precipitate was filtered and washed with THF. The concentration of the filtrate afforded the title compound as a light yellow solid. MS (ESI, pos. ion) m/z: 161 (M−NH3+1).

後処理

  1. customThe reaction was quenched with THF and H2O mixture (30 mL, THF:H2O=2:1)
  2. additionfollowed by the sequential addition of 5 N NaOH (10 mL) and H2O (100 mL)
  3. customthe temperature of the reaction lower than 5° C
  4. stirringThe reaction was stirred at RT for additional 5 h
  5. filtrationThe precipitate was filtered
  6. washwashed with THF

出典と根拠

ORDレコード
ord-bbc3411202db4524935e7a0e06ff839f
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07425631B2

反応ノート

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