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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632592Generated: November 4, 2026

2-Chloro-1,1-dimethoxyethane → HCID 20443243, compound

https://huagongshe.com/reaction/1632592

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1,1-dimethoxyethaneHCID 60986—
Reactant2,2-Dimethoxyethane-1-thiolHCID 14818260—
ReactantHCID 86739628HCID 86739628—
ProductHCID 20443243HCID 20443243—

Reaction Steps

Several processes for making 2-mercaptoacetaldehyde dimethylacetal (I, R1 =R2 =CH3) are reported by Parham et al., J. Am. Chem. Soc. 75, 2065-2069 (1953). These processes involve reaction of 2-chloroacetaldehyde dimethyl acetal with (1) benzylmercaptan sodium salt to produce benzyl-(1,1-dimethoxy ethyl)sulfide which was then reduced with sodium/ammonia to the desired acetal; (2) sodium sulfide to form 1,1,1',1'-tetramethoxyethyl disulfide followed by reduction of said disulfide using sodium/ammonia or lithium aluminum hydride; and (3) sodium polysulfide to give a mixture of polysulfides which was reduced with sodium/ammonia. A fourth process described in said reference comprises the action of potassium hydrosulfide on diethyl or dimethyl bromoacetal to produce the corresponding dialkyl mercaptoacetal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04476312
Source datasetuspto-grants-1984_10
ORD IDord-fab25363170c4d2f9f3952b228c597bf
Source noteuspto-grants-1984_10