Nitrogen → 12,12-Diethoxydodec-1-yne

온도

30 °C

To a dark solution of lithium acetylide, ethylenediamine complex (13.8 g, 134.90 mMol, (90%) Su: Aldrich) and NaI (0.78 g, 5.19 mMol, (99+%), Su: Acros) in DMSO (100 ml anhydrous (99.7%) Su: Acros) was charged 10-chloro-1,1-diethoxydecane 3 (27.48 g, 103.77 mMol Su: from step B) while maintaining reaction temperature around 30° C., under a blanket of N2. The addition funnel was rinsed with DMSO (15 ml, anhyrdrous, Su: Acros). The solution was monitored by GC for compound 3 consumption (compound 3<2.0 Area % by GC). After 4 hr stirring at 30° C., H2O (200 ml) were charged into the reaction mixture to quench the reaction. The aqueous layer was extracted with heptane (2×200 ml). The organic layer was filtered through a plug of Celite® 521 (15 g, Su: Sigma-Aldrich) one by one after phase separation. The combined filtrate was washed with a solution of H2O (100 ml) and brine (50 ml). The water in this organic solution was removed by azeotropic distillation under normal conditions by means of adding and removing heptane (repeat if necessary until KF=˜0.2%). The resultant solution was concentrated under reduced pressure (pot temperature ˜35° C.) to give 24.6 g of 12,12-diethoxydodec-1-yne 4 as an amber liquid (93% yield over steps A thru C, after C). This material was used without further purification. GC: column SP, Rt: 12.2 for 10-chloro-1,1-diethoxydecane 3, and Rt: 11.1 min for 12,12-diethoxydodec-1-yne 4 (<5 Area %). 1H NMR (CDCl3, 400 MHz): δ 4.48 (t, J=5.60, 1H), 3.6 (m, J=7.07 Hz, 2H), 3.5 (m, J=7.07 Hz, 2H), 2.18 (dt, J=7.10, 2.80 Hz, 2H), 1.94 (t, J=2.60 Hz, 1H), 1.6 (m, 2H), 1.52 (qn, J=7.2 Hz, 2H), 1.4 (m, 2H), 1.29 (br s, 10H), 1.20 (t, J=7.00 Hz, 6H).

1. temperaturewhile maintaining
2. customreaction temperature around 30° C.
3. washThe addition funnel was rinsed with DMSO (15 ml, anhyrdrous, Su: Acros)
4. customThe solution was monitored by GC for compound 3 consumption (compound 3<2.0 Area % by GC)
5. additionH2O (200 ml) were charged into the reaction mixture
6. customto quench
7. customthe reaction
8. extractionThe aqueous layer was extracted with heptane (2×200 ml)
9. filtrationThe organic layer was filtered through a plug of Celite® 521 (15 g, Su: Sigma-Aldrich) one by one
10. customafter phase separation
11. washThe combined filtrate was washed with a solution of H2O (100 ml) and brine (50 ml)
12. customThe water in this organic solution was removed by azeotropic distillation under normal conditions by means
13. additionof adding
14. customremoving heptane (repeat if necessary until KF=˜0.2%)
15. concentrationThe resultant solution was concentrated under reduced pressure (pot temperature ˜35° C.)

ORD 기록

ord-f501b8d94e8a40359ee21ced81284e82

출처 데이터셋

uspto-grants-2016_01

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US09233901B2