HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 20531215, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2,3-Dihydrobenzo(b)thiophene | HCID 78319 | — |
| Reactant | (2-Chloroacetamido)(hydroxy)acetic acid | HCID 23257102 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20531215 | HCID 20531215 | 65.3% |
Reaction Steps
N-Chloroacetyl-α-hydroxyglycine (6.5 g., 0.038 mole) was added to a cold, stirred mixture of concentrated sulphuric acid (1.5 ml.) and glacial acetic acid (15 ml.) followed, after five minutes, by the dropwise addition of 2,3-dihydrobenzo(b)thiophen (98%, 4.1 g., 0.03 mole). The reaction mixture was stirred at ambient temperature for five hours, then water (75 ml.) was added to the resulting suspension and the mixture thoroughly stirred. Filtration gave a solid which was washed successively with water, diethyl ether and hexane, then dried, to afford DL-α-chloroacetamido-2,3-dihydro-5-benzo(b)thienylacetic acid (5.6 g.), m.p. 173°-175° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04341792 |
| Source dataset | uspto-grants-1982_07 |
| ORD ID | ord-5be168416c9448a7818541a5f9996b55 |
| Source note | uspto-grants-1982_07 |