Acetyl chloride → HCID 67243086, compound

A solution of 2-bromo-7-methoxy-9H-xanthen-9-one (2.035 g, 6.7 mmol) in THF (67 ml) contained in a 250-mL RBF was cooled in a dry ice/acetone bath for 10 min to give a milky-white mixture. Trimethylsilyl methyllithium (10 ml of a 1.0 M solution in pentane, 10 mmol) was added dropwise over 5 min to give a clear orange solution. The mixture was stirred for 15 min, then acetyl chloride (0.76 ml, 11 mmol) was added dropwise, resulting in the formation of a clear, bright-yellow solution. The mixture was warmed to RT for 3 h, then an additional portion of acetyl chloride (0.25 mL) was added. The mixture was stirred for an additional 30 min before being diluted with saturated aqueous sodium bicarbonate solution (100 mL). The biphasic mixture was extracted with EtOAc (2×50 mL), and the combined organic extracts were dried over sodium sulfate, filtered, and evaporated to give a yellow solid that was used without further purification. MS m/z=303.0 [M+H]+. Calc'd for C15H12BrO2: 303.0.

1. temperaturewas cooled in a dry ice/acetone bath for 10 min
2. customto give a milky-white mixture
3. customto give a clear orange solution
4. customresulting in the formation of a clear, bright-yellow solution
5. stirringThe mixture was stirred for an additional 30 min
6. extractionThe biphasic mixture was extracted with EtOAc (2×50 mL)
7. dry with materialthe combined organic extracts were dried over sodium sulfate
8. filtrationfiltered
9. customevaporated
10. customto give a yellow solid that
11. customwas used without further purification

ORD record

ord-4024a112e33b4cbc9407273946056d07

Source dataset

uspto-grants-2014_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08883782B2