HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Methylene bis(chloroacetate)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Chloroacetic anhydride | HCID 10946 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | Methylene bis(chloroacetate) | HCID 86587291 | 57% |
Reaction Steps
Chloroacetic anhydride (12.75 g, 75 mmol), paraformaldehyde (2.25 g, 75 mmol) and conc. sulfuric acid (15 drops) are added to methylene chloride (15 ml). The mixture is stirred for 24 hrs. at 50° C. under nitrogen, whereafter the reaction mixture is extracted with saturated aqueous potassium carbonate until carbon dioxide emission ends. The organic layer is dried (MgSO4), evaporated to dryness and the residue is distilled (80° C., 0.15 mmHg) to yield 10.2 g (57%) product. 1H NMR (200 MHz, CDCl3): δ 4.1 (2×CH2Cl,s), 5.9 (CH2,s). 13C NMR (200 MHz, CDCl3): δ 41.1 (CH2Cl), 81.4 (O--CH2 --O), 166.4 (CO).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05919753 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-6e438629195d42f1b427efcc36b88f9d |
| Source note | uspto-grants-1999_07 |