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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
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 32112
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
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 1

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

Produkt 1

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

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

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).

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-bbc3411202db4524935e7a0e06ff839f
Quelldatensatz
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07425631B2

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