This post has been de-listed
It is no longer included in search results and normal feeds (front page, hot posts, subreddit posts, etc). It remains visible only via the author's post history.
Hey all
I am a PhD student in London and am asking the hive mind here for some advice.
After Christmas I am planning to carry out the following reaction, without any literature precedent by following a general protocol which I have been using over the last month now. The 3-Bromobenzylamine is sold as the .HCl salt. Naturally I will need an equivalent of base in the reaction to soak up the proton yet this base has to be non nucleophilic. My initial thoughts are to use equivalents of Potassium carbonate or a sterically hindered non nucleophilic base such as DBU. Can anyone give me some advice if you think these would be suitable or if you have any other suggestions.
Subreddit
Post Details
- Posted
- 3 years ago
- Reddit URL
- View post on reddit.com
- External URL
- reddit.com/r/OrganicChem...