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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391675Generated: November 2, 2026

Dimethylformamide → 1-[8(tert-butyl-dimethyl-silanyloxy)-6H-5-thia-1-aza-benzo[a]fluoren-11-yl]-ethanone

https://huagongshe.com/reaction/1391675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAcetyl chlorideHCID 6367—
ReactantSodium hydrideHCID 24758—
Reactant8-(Tert-butyl-dimethyl-silanyloxy)-6,11-dihydro-5-thia-11-aza-benzo[a]fluoreneHCID 59676059—
Product1-[8(tert-butyl-dimethyl-silanyloxy)-6H-5-thia-1-aza-benzo[a]fluoren-11-yl]-ethanoneHCID 69286054—

Reaction Steps

8-(tert-Butyl-dimethyl-silanyloxy)-6,11-dihydro-5-thia-11-aza-benzo[a]fluorene (170 mg, 0.462 mmoL) in DMF (2 mL) was treated with NaH (60%, 37 mg, 0.925 mmoL) at 0° C. Acetyl chloride (52 mg, 0.693 mmoL) was added dropwise into the reaction 30 minutes later. The reaction mixture was than slowly warmed to room temperature over 2 hours. The reaction was quenched with saturated NH4Cl. The residue was partitioned between CH2Cl2 and saturated NaHCO3. The aqueous phase was extracted two times with CH2Cl2. The organic layer from each extraction was combined, washed with water, brine, dried over anhydrous Na2SO4, filtered and concentrated to yield a brown oil. The oil was then purified by column chromatography (silica gel, hexanes:EtOAc 5:1 as eluent) to yield the title compound as a pale solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07338973B2
Source datasetuspto-grants-2008_03
ORD IDord-8f6a1b0d41034bfcb501afb1b40df72c
Source noteuspto-grants-2008_03