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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379481Generated: October 30, 2026

Methyl iodide → HCID 54180864, compound

https://huagongshe.com/reaction/1379481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactanttert-ButanolHCID 6386—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 54218849HCID 54218849—
SolventEthyl AcetateHCID 8857—
ProductHCID 54180864HCID 54180864471.2%

Reaction Steps

Potassium t-butoxide (0.22 g, 1.9 mmol) was added to 5 mL of t-butanol in a 25 mL round bottom flask. The (4aR)-(10bR)-10b-methyl-8-phenylthio-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]-quinolin-3-one, (0.183 g, 0.566 mmol) was added followed by methyl iodide while cooling briefly in an ice bath. The mixture was allowed to stir at room temperature for 18 h before diluting with ethyl acetate and filtering to remove inorganics. Filtrate was concentrated in vacuo to give a oil which was triturated in hexane/diethyl ether to facilitate crystallization. Recrystallization from ethyl acetate/hexane gave 0.90 g of white crystals: mp 109°-112°. FD MS 337 M +. Calcd for C21H23N1O1S1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670514
Source datasetuspto-grants-1997_09
ORD IDord-5cf8961c4f384f918c41a19d1178ebd4
Source noteuspto-grants-1997_09