HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418013Generated: November 1, 2026
2-Chloro-1,1-dimethoxyethane → HCID 20443243, compound
https://huagongshe.com/reaction/2418013
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloro-1,1-dimethoxyethane | HCID 60986 | — |
| Reactant | 2,2-Dimethoxyethane-1-thiol | HCID 14818260 | — |
| Reactant | HCID 86739628 | HCID 86739628 | — |
| Product | HCID 20443243 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04471139 |
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| Source dataset | uspto-grants-1984_09 |
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| ORD ID | ord-4ac2a633639b41a68d5d1d0e0233179d |
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| Source note | uspto-grants-1984_09 |
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