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?? ??:
81790-10-5
???:
(2-?????)??????
???(??):
(2-?????)??????
???:
(2-BROMOALLYL)TRIMETHYLSILANE
???(??):
(2-BROMOALLY)TRIMETHYLSILANE;(2-BROMOALLYL)TRIMETHYLSILANE;2-BROMO-3-(TRIMETHYLSILYL)PROPENE;(2-Bromoallyl)trimethylsilane >2-Bromo-3-trimethylsilyl-1-propene;Silane,(2-bromo-2-propen-1-yl)trimethyl-; (2-Bromo-2-propen-1-yl)(trimethyl)silane;(2-BROMOALLYL)TRIMETHYLSILANE, TECH., 90 %
CBNumber:
CB7292730
???:
C6H13BrSi
??? ??:
193.16
MOL ??:
81790-10-5.mol
MSDS ??:
SDS

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?? ?
82-85 °C/60 mmHg (lit.)
??
1.121 g/mL at 25 °C (lit.)
???
n20/D 1.462(lit.)
???
87 °F
?? ??
2-8°C
???
???, ???, ???, ?????????, ??? ???? ?? ??????.
??? ??
liquid
BRN
3600686
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? Xi
?? ???? ?? 10-36/37/38
????? 16-26-36
????(UN No.) UN 1993 3/PG 3
WGK ?? 3
F ?????? 8-10
HS ?? 2931.90.9010
?? ?? 3.2
???? III
????(GHS): GHS hazard pictogramsGHS hazard pictograms
?? ?: Warning
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H226 ??? ?? ? ?? ??? ?? ?? 3 ??
H315 ??? ??? ??? ????? ?? ????? ?? 2 ?? GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 ?? ?? ??? ??? ?? ? ?? ?? ??? ?? ?? 2A ?? GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 ?? ???? ??? ? ?? ?? ???? ?? - 1? ??;???? ?? ?? 3 ?? GHS hazard pictograms
??????:
P210 ?·???·??·????? ????? - ?? ???.
P302+P352 ??? ??? ??? ?? ????.
P305+P351+P338 ?? ??? ? ?? ?? ???? ????. ???? ?????? ?????. ?? ????.
NFPA 704
3
0 0

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bp 46–50°C/20 mmHg,64–65°C/38– 39 mmHg.

??

2-Bromo-3-trimethylsilyl-1-propene can be used as synthon for CH2=C?CH2TMS1–3 and CH2=CBrC?H2;2 for synthesis of 1-trimethylsilylmethyl-substituted 1,3-butadienes.
The 1-trimethylsilylmethylvinyl anion CH2=C(M)CH2TMS (2) (M = Li, Mg, Cu, etc.), readily prepared from 2-bromo-3-trimethylsilyl-1-propene (1) under typical conditions, allows the introduction of the synthetically useful 1-trimethylsilylmethylvinyl group to a wide variety of substrates. Ring opening of 1-butene oxide with the Grignard reagent (2) (M = MgBr) in the presence of copper(I) iodide gives only one regioisomer. Subsequent desilylative oxidation of this allyl alcohol to α-methylene-γ-lactones provides further utility of (1) as a 1-hydroxymethylvinyl anion equivalent, i.e. CH2=?C?CH2OH (eq 1).Alternatively, the alcohol from trans-2,3-epoxybutane provides a route to the unstable sixmembered β,γ-unsaturated lactone (eq 2).The copper-catalyzed 1,4-addition to the typically unreactive mesityl oxide proceeds smoothly. The versatility of the allylsilane moiety is again illustrated in the ethylaluminum dichloride-induced cyclization of the adduct to a tertiary cyclopentanol in high yield (eq 3).versatility of the allylsilane moiety

?? ??

reaction of 2,3-dibromopropene with lithium (trimethylsilyl)cuprate in HMPA at 0°C (63–90%);(2) reaction of 2,3-dibromopropene with trichlorosilane in the presence of trichlorosilane and copper( I) chloride, followed by treatment with methylmagnesium bromide (63–71%).

Purification Methods

It is fractionally distilled through an efficient column. It is flammable. [Trost & Chan J Am Chem Soc 104 3733 1982, Trost & Coppola J Am Chem Soc 104 6879 1982.]

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