Acetic Acid → 3-Chloro-2-hydroxypropyl acetate

Epichlorohydrin (187 g, 2.0 mol) was added dropwise over a 75 minute period to a mechanically stirred suspension of 10.0 g (0.062 mol) of anhydrous ferric chloride in 138 mL (2.4 mol) of glacial acetic acid at 0°-10° C. After the addition was completed, the reaction mixture was stirred one hour and was allowed to stand at room temperature for two days. Anhydrous sodium acetate (5.1 g, 0.062 mol) was added and excess acetic acid was then removed in vacuo. The mixture was diluted with 200 mL of methylene chloride and filtered through Celite™ (i.e. diatomaceous earth). The solution was washed with 10% potassium carbonate and dried over potassium carbonate and sodium sulfate. Removal of the methylene chloride in vacuo gave 275 g of crude 3-chloro-2-hydroxy-1-propyl acetate, and an additional 9 g was recovered by extracting the potassium carbonate solution with methylene chloride (93% crude yield). This material was used without purification in the subsequent step. 1H NMR (CDCl3) δ2.10 (s, 3H, --COCH3); 3.80 (m, 6H, --CH2CH(OH)CH2 --); IR (film) 3500 (--OH); 1735 cm-1 (--COCH3).

1. additionAfter the addition
2. waitto stand at room temperature for two days
3. customexcess acetic acid was then removed in vacuo
4. additionThe mixture was diluted with 200 mL of methylene chloride
5. filtrationfiltered through Celite™ (i.e. diatomaceous earth)
6. washThe solution was washed with 10% potassium carbonate
7. dry with materialdried over potassium carbonate and sodium sulfate
8. customRemoval of the methylene chloride in vacuo

ORD record

ord-c57f693d2c8d469ab504dd7f4561c124

Source dataset

uspto-grants-1983_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04395561