HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754894Generated: October 28, 2026
2-(Methyldithio)isobutyraldehyde → HCID 86671286, compound
https://huagongshe.com/reaction/1754894
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Methyldithio)isobutyraldehyde | HCID 106217 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13401257 | HCID 13401257 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86671286 | HCID 86671286 | 65% |
Reaction Steps
(5-amino-1,3-phenylene)dimethanol (2.5 g, 16.32 mmol) and 2-(methyldithio)isobutyraldehyde (2.347 ml, 16.32 mmol) were stirred at ambient temperature in absolute ethanol (82 ml) until completely dissolved (3 hours). The mixture was cooled to 0° C. in an ice bath and sodium borohydride (0.741 g, 19.59 mmol) was added. The reaction was stirred for 1 hour at 0° C., and was then quenched slowly with cold 5% HCl solution. The mixture was diluted with dichloromethane and the pH was adjusted to pH=8 with saturated sodium bicarbonate solution then extracted with dichloromethane and then washed with brine. The organic extracts were dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. Purification by silica gel chromatography (MeOH/DCM) yielded (5-(2-methyl-2-(methyldisulfanyl)propylamino)-1,3-phenylene)dimethanol (3 g, 65%) as a white solid. 1H NMR (400 Hz, CDCl3): δ6.62 (s, 1H), 6.54 (s, 2H), 4.53 (s, 4H), 3.13 (s, 2H), 2.30 (s, 3H), 1.32 (s, 6H). See FIG. 47.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169272B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-c2c451429a244932b59cc84bd9b62ca5 |
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| Source note | uspto-grants-2015_10 |
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