HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromo-5,5-dimethylhydantoin → 4-Bromomethylphenyl 2,3,4,6-tetra-O-acetyl-alpha-D-galactopyranoside
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromo-5,5-dimethylhydantoin | HCID 6479 | — |
| Reactant | 4-Methylphenyl 2,3,4,6-tetra-O-acetyl-alpha-D-galactopyranoside | HCID 54141638 | — |
| Product | Methanol | HCID 887 | 76% |
| Product | 4-Bromomethylphenyl 2,3,4,6-tetra-O-acetyl-alpha-D-galactopyranoside | HCID 53928040 | 422.9% |
Reaction Steps
1.4 g (3.2 mmoles) of 4-methylphenyl 2,3,4,6-tetra-O-acetyl-α-D-galactopyranoside (71) and 0.46 g (1.6 mmole) of 1,3-dibromo 5,5-dimethylhydantoine are added in 100 ml of carbone tetrachloride, and the mixture est refluxed under irradiation with light (1 000 W) for 15 minutes. After cooling, the reaction medium is filtered and the filtrate is then evaporated to dryness. 3.5 g of 4-bromomethylphenyl 2,3,4,6-tetra-O-acetyl-α-D-galactopyranoside (72) are isolated by crystallization from methanol (yield=76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05561119 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-084f5d8f190e4bb0a3d0ddded00d656d |
| Source note | uspto-grants-1996_10 |