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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158060Generated: October 30, 2026

Chlorotrimethylsilane → HCID 58929517, compound

https://huagongshe.com/reaction/1158060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantN-bromobutanimideHCID 67184—
ReactantLithium diisopropylamideHCID 2724682—
ReactantMethyl (oxan-4-yl)acetateHCID 46738768—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58929517HCID 58929517—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a dry 250 mL round-bottomed flask was added 2.20 g of methyl 2-(tetrahydro-2H-pyran-4-yl)acetate (0.014 mol) and 100 mL of dry THF. This solution was cooled to −78° C. and LDA (2.0 M in THF/heptane/ethyl benzene, 10.4 mL, 0.021 mol) was added. The resulting brown solution was stirred at −78° C. for 45 min. TMSCl (3.22 g, 3.5 mL, 0.028 mol) was then added at −78° C., and the reaction mixture was then warmed to room temperature. After being re-cooled to −78° C., N-bromosuccinimide (4.94 g, 0.028 mol) was added to the reaction mixture, and the resulting suspension was allowed to slowly warm to room temperature where it continued to stir for an additional 1.5 h. The suspension was then filtered thru a pad of SiO2 using diethyl ether as the eluant. Purification of the filtrate by column chromatography (SiO2 gel, 10:1 to 4:1 hexanes/ethyl acetate) delivered the desired α-bromo ester, which was used in subsequent steps without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807700B2
Source datasetuspto-grants-2010_10
ORD IDord-91eab41c4f7f49798fb89f1cab005f54
Source noteuspto-grants-2010_10