HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosulfonic acid → HCID 20201777, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | HCID 14468440 | HCID 14468440 | — |
| Product | HCID 20201777 | HCID 20201777 | 24% |
Reaction Steps
There was reacted 1.0 g (5.8 mmole) of 2-acetyl-7-methylbenzofuran with chlorosulfonic acid as in Example 1, yielding 0.36 g of 2-acetyl-4-chlorosulfonyl-7-methylbenzofuran (yield: 24%, MS (m/z): 232 (M+), 257, 237 and 173). The obtained chlorosulfonyl compound was reacted with glycine ethyl ester hydrochloride as in Example 1 to give an ester compound (yield: 73%, MS (m/z): 339 (M+), 266, 237 and 173), which was then hydrolyzed to give 2-acetyl-4-(N-carboxymethylsulfamoyl)-7-methylbenzofuran (yellow plates, yield: 71%). The physical constants are shown in Table 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04666931 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-84c80c536bdc494e952337dceda5cb29 |
| Source note | uspto-grants-1987_05 |