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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402270Generated: October 31, 2026

Acetyl chloride → HCID 68709063, compound

https://huagongshe.com/reaction/1402270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 44603824HCID 44603824—
SolventMethanolHCID 887—
ProductHCID 68709063HCID 6870906387.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of Intermediate 85b (6.39 g, 17.9 mmol) and sodium methoxide (580 mg, 10.8 mmol) in MeOH (100 mL) was stirred at RT for 18 h. The mixture was cooled to 0° C., then acetyl chloride (28.4 g, 359 mmol) added. This mixture was stirred at reflux for 1 h, then cooled and concentrated in vacuo. The residue was divided, applied to SCX-2 cartridges (3×70 g) and washed with MeOH. The product was eluted with 2M NH3 in MeOH; concentration in vacuo gave the title compound as a pale yellow oil (3.92 g, 87%). 1H NMR (400 MHz, CDCl3): 1.62-1.86 (3H, m), 1.07-2.13 (1H, m), 2.48 (1H, br s), 2.93-3.11 (2H, m), 3.69-3.78 (4H, m), 4.53 (1H, d, J 12.9), 4.55 (1H, d, J 12.9), 7.21-7.37 (5H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907094B2
Source datasetuspto-grants-2014_12
ORD IDord-bfaccf41b87147b5a9b442d038db79b5
Source noteuspto-grants-2014_12