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Benzene → Previtamin D3

HRID 2413692
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2413692
[CH3:1][CH:2]([CH2:4]/[CH:5]=[CH:6]/[C@H:7]([C@@H:9]1[C@:26]2([CH3:27])[C@H:12]([C:13]3[C@H:23]([CH2:24][CH2:25]2)[C@:21]2([CH3:22])[C:16]([CH2:17][C@H:18]([OH:28])[CH2:19][CH2:20]2)=[CH:15][CH:14]=3)[CH2:11][CH2:10]1)[CH3:8])[CH3:3].C1C=CC=CC=1>CCOCC>[CH3:22][C:21]1[CH2:20][CH2:19][C@H:18]([OH:28])[CH2:17][C:16]=1/[CH:15]=[CH:14]\[C:13]1[C@@H:12]2[CH2:11][CH2:10][C@H:9]([C@@H:7]([CH2:6][CH2:5][CH2:4][CH:2]([CH3:3])[CH3:1])[CH3:8])[C@@:26]2([CH3:27])[CH2:25][CH2:24][CH:23]=1
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Komponenten

4

Edukt 2

HCID 241BenzeneHCID 70410550HCID 70410550, Verbindung

Produkt 1

HCID 5281058Previtamin D3Ausbeute 40,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

(5Z,7E,22E)-9,10-Secocholesta-5,7,10(19),22-tetraen-3α-ol (5) A solution of compound (4) (100 mg, 0.26 mmol) in ether (120 ml)-benzene (30 ml) mixture was degassed with argon for 40 min. The solution was irradiated at 0° C. for 13 min in a quartz immersion well equipped with UV lamp and filter. The solvent was removed under reduced pressure and the residue separated by HPLC, using 1% 2-propanol in hexane as eluent to obtain the pure previtamin D derivative (40.4 mg, 40%) which was collected at 24 ml; NMR δ 0.72 (3H, s, 18-H3), 0.87 (6H, d, J=6.7 Hz, 26-H3 and 27-H3), 1.04 (3H, d, J=6.8 Hz, 21-H3), 1.65 (3H, s, 19-H3), 3.91 (1H, m, 3-H), 5.28 (2H, br m, 22-H and 23-H, 5.50 (1H, m, 11-H), 5.69 and 5.96 (2H, AB q, J=12.5 Hz, 7-H and 6-H); UV λmax 260.5 nm; λmin 234 nm. The previtamin (40 mg, 0.1 mmol) in ethanol (100 ml) was heated under reflux for 3 h. After removal of solvent, the product mixture was separated by HPLC (elution with 1% 2-propanol in hexane). The yield of the vitamin (5) (collected at 34 ml) was 30.8 mg (77%) mp (hexane) 99°-101° C.; NMR δ 0.56 (3H, s, 18-H3), 0.88 (6H, d, J=6.7 Hz, 26-H3 and 27-H3), 1.02 (3H, d, J=6.6 Hz, 21-H3), 3.96 (1H, m, 3-H), 4.82 and 5.05 (2H, each narr. m, 19-H2), 5.27 (2H, br m, 22-H and 23-H), 6.03 and 6.24 (2H, ABq, J=11.4 Hz, 7-H and 6-H; UV λmax 265 nm, λmin 228 nm; IR: 3420,1458,1441,1378,1366,1050,970,943,891,862 cm-1 ; mass spectrum, m/e (M+, 22), 349 (M+ -H2O-Me, 4), 271 (M+ -side chain, 8), 253 (M+ -side chain-H2O, 13), 136 (100), 118 (80).

Aufarbeitung

  1. customwell equipped with UV lamp
  2. filtrationfilter
  3. customThe solvent was removed under reduced pressure
  4. customthe residue separated by HPLC

Quellen und Nachweise

ORD-Eintrag
ord-8e4c3e5c476746babf78f8eb85019fed
Quelldatensatz
uspto-grants-1988_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04719204

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