HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium methanethiolate → 2,2-Dimethyl-5-[2-(methylthio)acetyl]-1,3-benzodioxole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | 2-Bromo-1-(2,2-dimethyl-1,3-benzodioxol-5-yl)ethanone | HCID 14373073 | — |
| Reactant | alpha-Methylthioacetophenone | HCID 18968240 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,2-Dimethyl-5-[2-(methylthio)acetyl]-1,3-benzodioxole | HCID 14373074 | — |
Reaction Steps
The procedure is as in Example 4 for the preparation of α-methylthioacetophenone, starting with a stirred solution of 5-(2-bromoacetyl)-2,2-dimethyl-1,3-benzodioxole (14.9 g) in methanol (150 cc). Sodium methanethiolate (3.8 g) is added in the course of 5 minutes at a temperature in the region of 20° C., and the mixture is left with stirring for 15 hours at the same temperature. 2,2-Dimethyl-5-[2-(methylthio)acetyl]-1,3-benzodioxole (11 g) is thereby obtained, and is used in the crude state in the subsequent syntheses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04886835 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-fcb6d5b3eb434a7597996d1bdf9306cf |
| Source note | uspto-grants-1989_12 |