HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-(3-Bromopropyl)-5-formyloxy-4,6,7-trimethyl-1,3-benzoxathiole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-(3-Hydroxypropyl)-4,6,7-trimethyl-2H-1,3-benzoxathiol-5-ol | HCID 127577 | — |
| Product | 2-(3-Bromopropyl)-5-formyloxy-4,6,7-trimethyl-1,3-benzoxathiole | HCID 14802180 | — |
Reaction Steps
1.5 g of triphenylphosphine was dissolved in 3 ml of dimethylformamide, and then a solution of 0.9 of bromine in 2 ml of dimethylformamide was added dropwise. The mixture was allowed to react for 30 minutes at room temperature, after which 0.5 g of 3-(5-hydroxy-4,6,7-trimethyl-1,3-benzoxathiole-2-yl)propanol (prepared as described in Example 71) was added. The reaction mixture was allowed to react for a further 20 hours at room temperature. The same treatment and separation procedures as described in Example 75 were carried out. From the fraction eluted first was obtained 2-(3-bromopropyl)-5-formyloxy-4,6,7-trimethyl-1,3-benzoxathiole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04691027 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-19a0119ff8914469b3cedddde0664844 |
| Source note | uspto-grants-1987_09 |