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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040470Generated: October 31, 2026

Acetyl chloride → HCID 59676138, compound

https://huagongshe.com/reaction/2040470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 619571HCID 619571—
SolventDichloromethaneHCID 6344—
ProductHCID 59676138HCID 59676138—

Reaction Steps

Acetyl chloride (0.064 mL, 0.896 mmoL) in CH2Cl2 (2 mL) was treated with 8-methoxy-6,11-dihydro-5-oxa-11-aza-benzo[a]fluorene (150 mg, 0.598 mmoL) followed by Et3N (0.896 mmol., 0.125 mL) at 0° C. The reaction mixture was then slowly warmed to room temperature over 2 hours. The reaction mixture was then partitioned between CH2Cl2 and saturated NaHCO3. The aqueous phase was extracted two times with CH2Cl2. The organic layers from the two extractions were then combined, washed with water and brine, dried over anhydrous Na2SO4, filtered and concentrated to yield a brown oil. The crude material was then purified by column chromatography (silica gel, hexanes:EtOAc 3:1 as eluent) to yield the title compound as a pale solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580840B2
Source datasetuspto-grants-2013_11
ORD IDord-395a93bd0bc84c8492af4682f1281f59
Source noteuspto-grants-2013_11