HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 178459584, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 178476994 | HCID 178476994 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Product | HCID 178459584 | HCID 178459584 | — |
Reaction Steps
The reaction mixture from step 1 was cooled under nitrogen and then diluted with 200 g. of methylene chloride. Then, 289 g. of acetic anhydride, along with a catalyst of 0.5 g. of 4-dimethylaminopyridine, were added to the reaction mixture. The reaction mixture was stirred for 1 hour at which time NMR analysis of a vacuum stripped aliquot indicated complete conversion to the desired thioacetate. The product was distilled at 132°-134° C. at 20 mm Hg to yield 355 g. of product (80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05290956 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-12dab1fe23fd4888acfbb6da2a42a8c5 |
| Source note | uspto-grants-1994_03 |