HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028875Generated: October 31, 2026
Formaldehyde → 2-Nitro-2-(4-octylphenethyl)propane-1,3-diol
https://huagongshe.com/reaction/1028875
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 3-Nitro-1-(4-octylphenyl)propyl acetate | HCID 56968057 | — |
| Product | 2-Nitro-2-(4-octylphenethyl)propane-1,3-diol | HCID 66837276 | — |
Reaction Steps
To a mixture of paraformaldehyde (0.13 mol, 9 eq), 4 ml (1.5 eq) of triethylamine in 40 ml of 1,4-dioxane, 3-nitro-1-(4-octylphenyl)propyl acetate (13) (5 g, 0.015 mol) in 50 ml of 1,4-dioxane was added dropwise with stirring at RT, the mixture was slowly heated to 70° C., and stirred for 24 h at this temperature, under TLC control. To the reaction mixture was added water and the mixture, pH adjusted to ˜9-10 and stirred 16 h at 40° C. for deprotection (TLC and HPLC monitoring). After reaction completion (˜2-3 h) the mixture was extracted with ethyl acetate and washed successively with 1 N HCl, sodium bicarbonate solution and brine. The ethyl acetate solution was dried over sodium sulfate and concentrated. The residue was pure enough for transformation to the next step or can be purified by crystallization or silica gel column chromatography using hexane-ethyl acetate as eluent to afford a white solid with mp. 80-82° C., ESIMS 376.2 [M+Na]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735627B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-ff6d7c37f5e84f76985ad4b5c83062ac |
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| Source note | uspto-grants-2014_05 |
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