Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598417Generated: November 2, 2026

Chlorotrimethylsilane → HCID 18932641, compound

https://huagongshe.com/reaction/1598417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDiisopropylamineHCID 7912—
ReactantSodium BicarbonateHCID 516892—
ReactantLithium diisopropylamideHCID 2724682—
ReactantN-BromosuccinamideHCID 9834204—
ReactantHCID 10966498HCID 10966498—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18932641HCID 18932641—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of methyl (5,8-dimethoxy-3,4-dihydrobenzo [2,3-c] pyran-3-yl) ketone (1.905 g, 8.04 mmol) and trimethylsilyl chloride (1,530 μl, 12.0 mmol) in tetrahydrofuran (48 ml) under nitrogen, at -78° C., was slowly added lithium diisopropyl amide (diisopropyl amine 10.71 mmol, n-butyl lithium 4.26 ml of a 2.5M solution in tetrahydrofuran, and 6.0 ml of tetrahydrofuran). After stirring for 10 minutes the temperature was raised to 0° C., and stirring was continued for 10 more minutes. Solvent was removed and the crude product was dissolved in 48 ml of tetrahydrofuran, N-bromosuccinamide (1,716 mg, 9.66 mmol) was added slowly to the solution. After 10 minutes, the reaction system was worked up with saturated aqueous sodium bicarbonate and washed with brine. The titled compound was obtained following flash chromatography (hexanes:ethyl acetate, 9:1) of the crude product. 1H NMR (benzene-d6, 250 MHz) -- : 2.68 (dd, 1H,HCHa), 3.16 (dd,1H,HCHe), 3.28 (s,3H,OCH3), 3.32 (s,3H,OCH3), 3.73 (dd,1H,J=4.0,11.5 Hz,CH), 3.81 (dd,2H,CH2Br), 4.51 (d,1H, J=15.8 Hz, HCHaO), 5.05 (d,1H,J=15.8 Hz,HCHeO), 6.335 (dd,2H,ArH),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736523
Source datasetuspto-grants-1998_04
ORD IDord-a805fdbc02244aa4bf67412096484a88
Source noteuspto-grants-1998_04