HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 2-(Acetoxymethyl)-4-bromobutyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1,4-Butanediol, 2-[(acetyloxy)methyl]-, 1-acetate | HCID 10176610 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Acetoxymethyl)-4-bromobutyl acetate | HCID 10264950 | 993.2% |
Reaction Steps
A mixture of 2-acetoxymethyl-4-hydroxy-but-1-yl acetate (10 g, 49 mmol), triphenyl phosphine (19.25 g, 73 mmol) and carbon tetrabromide (24.4 g, 73 mmol) was stirred for 18 hours at 4° C. in dimethylformamide (150 ml). The solvent was then evaporated, and the residue purified by column chromatography on silica gel, eluting with ether-light petroleum 2:3 to afford 2-acetoxymethyl-4-bromobut-1-yl acetate as a pale oil (130 g, 99%). δH (CDCl3) 1.73-2.56 (3 H, m, CHCH2CH2), 2.04 (6 H, s, 2×OCOCH3), 3.44 (2 H, t, CH2Br), 4.04 (4 H, d, 2×CH2OCOCH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05075445 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-7d188c8a322f4480923e05066109588b |
| Source note | uspto-grants-1991_12 |