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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455697Generated: October 30, 2026

Bromide ion → HCID 69049226, compound

https://huagongshe.com/reaction/1455697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantWaterHCID 962—
ReactantHCID 11858598HCID 11858598—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69049226HCID 69049226—

Reaction Conditions

Temperature25 °C

Reaction Steps

5.4 g (15.3 mmol) of methyltriphenylphosphate [sic] bromide are added to a suspension of 1.75 g (14.9 mmol) of potassium tert-butoxide in 20 ml of tetrahydrofuran. The reaction medium is stirred for 1 hour at 25° C. and then cooled to 0° C. A solution of 4.5 g (12.9 mmol) of ethyl4-(6-hexyl-3-oxoindan-5-yloxy)butyrate is added. The mixture is stirred for 16 hours at 25° C., poured into water and extracted with ether. The organic phase is dried (Na2SO4) and concentrated under reduced pressure (oil). Purification by flash chromatography (80/20 heptane/ethyl acetate) gives an orange oil (3.5 g; 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482484B2
Source datasetuspto-grants-2009_01
ORD IDord-132bbf1e362043e3bccaeb0898f4da83
Source noteuspto-grants-2009_01