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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754894Generated: October 28, 2026

2-(Methyldithio)isobutyraldehyde → HCID 86671286, compound

https://huagongshe.com/reaction/1754894

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methyldithio)isobutyraldehydeHCID 106217—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13401257HCID 13401257—
SolventEthanolHCID 702—
ProductHCID 86671286HCID 8667128665%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169272B2
Source datasetuspto-grants-2015_10
ORD IDord-c2c451429a244932b59cc84bd9b62ca5
Source noteuspto-grants-2015_10