HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-[(1,3-Benzodithiol-2-ylidene)amino]-2-thioxo-4-thiazolidinone → 3-[(1,3-Benzodithiol-2-ylidene)amino]-5-pentylidene-2-thioxo-4-thiazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-[(1,3-Benzodithiol-2-ylidene)amino]-2-thioxo-4-thiazolidinone | HCID 12494993 | — |
| Catalyst | Piperidine, acetate | HCID 9793820 | — |
| Solvent | Pentanal | HCID 8063 | — |
| Product | 3-[(1,3-Benzodithiol-2-ylidene)amino]-5-pentylidene-2-thioxo-4-thiazolidinone | HCID 57324532 | 89.6% |
Reaction Steps
A slurry of 2.0g of 3-[(1,3-benzodithiol-2-ylidene)amino]- 2-thioxo-4-thiazolidinone (see example 37), valeraldehyde (10 ml, excess) and acetic acid/piperidine (2:1) (10 drops) in anhydrous slyme (400 ml) is heated at reflux for eighteen hours. The reaction mixture is chilled in an ice bath and the resultant precipitate collected by filtration. This precipitate (1.6 g) is recrystallized from 50 ml of dimethylformamide to yield 1.1 g of the title compound, melting point 210°-212° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04107175 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-ee6cda9cab894396a20a06a768418928 |
| Source note | uspto-grants-1978_08 |