HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 86706083, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 13157916 | HCID 13157916 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 86706083 | HCID 86706083 | 14% |
Reaction Steps
A solution of ethyl 2,2-bis(hydroxymethyl)-3-oxobutanoate (75 g, 0.39 mol) and 40% formaldehyde (360 mL) in concentrated hydrochloric acid (360 mL) was heated at 50° C. for 17 h. The two-phase solution was cooled to room temperature and extracted with ethyl acetate (2×200 mL). The combined organic phases were washed with water, dried over magnesium sulfate, and evaporated to give a residue, which was purified by flash column chromatography eluting with a continuous gradient of petroleum ether/ethyl acetate 15:1 to 9:1 to afford the title compound (33 g, 14%, 2 steps) as a colorless oil. 1H NMR (400 MHz, CDCl3) δ 1.25 (m, 3H), 2.31 (s, 3H), 4.25-4.19 (m, 4H), 4.35 (d, J=12.0 Hz, 2H), 4.77 (d, J=6.0 Hz, 1H), 4.82 (d, J=6.0 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062092B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-652ace6fc9764c81a0d0ca68132934e2 |
| Source note | uspto-grants-2015_06 |