Diethyl Ether → HCID 68854392, Verbindung

HRID 2101665

Reaktionsgleichung

Reaktionsgleichung von HRID 2101665
[C:1]([O:5][C:6]([N:8]1[C@H:12]([CH:13]([F:16])[CH:14]=[CH2:15])[CH2:11][O:10][C:9]1([CH3:18])[CH3:17])=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:19]=[CH:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31]CC.CCOCC.CCCCCC>C(Cl)Cl.Cl[Ru](=C1N(C2C(C)=CC(C)=CC=2C)CCN1C1C(C)=CC(C)=CC=1C)(Cl)(=CC1C=CC=CC=1)[P](C1CCCCC1)(C1CCCCC1)C1CCCCC1>[C:1]([O:5][C:6]([N:8]1[C@H:12]([CH:13]([F:16])[CH:14]=[CH:15][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH3:19])[CH2:11][O:10][C:9]1([CH3:18])[CH3:17])=[O:7])([CH3:4])([CH3:3])[CH3:2]

Komponenten

7

Edukt 4

HCID 3283Diethyl EtherHCID 8058HexaneHCID 259131-PentadeceneHCID 57801768tert-Butyl-(4S)-4-(1-fluoroprop-2-en-1-yl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

Produkt 1

HCID 68854392HCID 68854392, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 178425456HCID 178425456, VerbindungKatalysatorHCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

tert-Butyl-(4S)-4-(1-fluoroprop-2-en-1-yl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate (0.036 g, 0.14 mmol) and 1-pentadecene (0.2 ml, 5 eq) were solubilised in anhydrous CH2Cl2 (2.5 ml) under an atmosphere of nitrogen, in a sealed tube. Grubbs 2nd Generation catalyst (0.006 g, 2 mol %) was added as a solid, and the reaction mixture was allowed to stir for 36 hours at 100° C., with the reaction monitored by t.l.c. (ether:hexane, 1:19). The reaction mixture was then cooled to room temperature and concentrated under reduced pressure. Purification by flash chromatography (ether:hexane, 1:19) afforded the product (0.062 g, quantitative yield) and a mixture of compounds of varying alkyl chain length. Tentative analysis of this compound describes a mixture of products. m/z: HRMS required for C26H48FNO3 mass is 441.3600, found 441.3618 as major compound, also found 413.3164, 427.3433, 455.3875 and 469.3886 as minor products; IR (film) νmax (cm−1) 2926, 1704, 1386; 1H NMR (CDCl3, 400 Mhz) δ=5.81 (m, 1H, H8), 5.51 (m, 1H, H7), 5.10 and 4.94 (2 m, H6erythreo, threo), 4.08 (m, 1H, H4), 3.94 (m, 2H, H5,5′), 2.04 (m, 2H, H9,9′), 1.48 (m, 15H, NCOOC(CH3)3 and —OC(CH3)2N—), 1.25 (br s, 22H, (CH2)11), 0.88 (t, J=7.0, 3H, CH3, H21); 13C-NMR (CDCl3, 100.6 MHz) δ=152.4 (—NCOO—), 136.9 (CH, C8), 125.2 (CH, C7), 94.4 (CH, C6), 93.9 (OC(CH3)2N), 80.4 (OC(CH3)3), 63.4 (CH, C4), 60.4 (CH2, C5), 31.6, 31.9, 29.7, 22.7, 21.0 (12C, CH2, (CH2)12), 28.4 (CH3, OC(CH3)3), 26.9 and 24.7 (CH3, —OC(CH3)2N—), 14.1 (CH3, (CH2)12CH3)); 19F-NMR (CDCl3, 400 MHz) δ=major compounds −183.0, −186.0, minor compounds −175.6, −177.7, −192.6, −194.6;

Aufarbeitung

  1. temperatureThe reaction mixture was then cooled to room temperature
  2. concentrationconcentrated under reduced pressure
  3. customPurification by flash chromatography (ether:hexane, 1:19)

Quellen und Nachweise

ORD-Eintrag
ord-2b87946b2c2b412696607790ee978cbf
Quelldatensatz
uspto-grants-2009_08
Patentnummer
US07572928B2

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