HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → Ethyl 4,5-dihydro-4-oxothiopyrano[3,2-b]indole-5-acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Thiopyrano[3,2-b]indol-4(5H)-one | HCID 20326608 | — |
| Product | Ethyl 4,5-dihydro-4-oxothiopyrano[3,2-b]indole-5-acetate | HCID 20326604 | — |
Reaction Steps
By the same method as described in Example 7, 4.8 g of thiopyrano[3,2-b]indol-4(5H)-one is alkylated with ethyl bromoacetate to give 6.0 g of product, mp 163°-165° C, after recrystallization from ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04064123 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-40fd097d08904239b6a1e38247841b49 |
| Source note | uspto-grants-1977_12 |