Pyridine → 2-adamantyl Chloroformate

HRID 233630

Reaktionsgleichung

Reaktionsgleichung von HRID 233630
[CH:1]12[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH:2]1[OH:11])[CH2:8]2.[Cl:12][C:13]([O:16]C(=O)OC(Cl)(Cl)Cl)(Cl)Cl.N1C=CC=CC=1>ClCCl>[Cl:12][C:13]([O:11][CH:2]1[CH:3]2[CH2:9][CH:7]3[CH2:6][CH:5]([CH2:10][CH:1]1[CH2:8]3)[CH2:4]2)=[O:16]

Komponenten

5

Edukt 3

HCID 1049PyridineHCID 641492-AdamantanolHCID 94429Triphosgene

Produkt 1

HCID 108785372-adamantyl ChloroformateAusbeute 251,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

A solution of 2-adamantanol (10.1 g, 66.5 mmol) in dichloromethane (200 mL) was cooled in an ice bath. Bis(trichloromethyl)carbonate (triphosgene) (7.55 g, 25.4 mmol) was added followed by dropwise addition of pyridine (6.2 mL, 77 mmol) at such a rate that the temperature remained below 20° C. After a further 10 minutes the mixture was warmed to room temperature and stirred for a further 2.5 hours. The dichloromethane was removed in vacuo without heating and the residue slurried with ethyl acetate (50 mL). The pyridinium hydrochloride was filtered off and the filtrate evaporated to dryness without heating to yield 2-adamantylchloroformate (76) (13.7 g, 96%); δ H (300M Hz, CDCl3, 1.48-2.32 (14H, m, adamantyl), 5.01 (1H, t, J 3 Hz, adamantyl 2-H); (lit. ,2 δ H (CCl4) 1.3-2.4 (14H, m), 4.95 (1H, s).

Aufarbeitung

  1. customremained below 20° C
  2. customThe dichloromethane was removed in vacuo
  3. temperaturewithout heating
  4. filtrationThe pyridinium hydrochloride was filtered off
  5. customthe filtrate evaporated to dryness
  6. temperaturewithout heating

Quellen und Nachweise

ORD-Eintrag
ord-e983796454df48f3abd22062c15dbbfc
Quelldatensatz
uspto-grants-1997_01
Patentnummer
US05593967

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